Ordin nr. 1301/500/2008 din 11 iulie 2008 Partea a ii-a


Se aplică tuturor denumirilor comerciale, formelor farmaceutice şi concentraţiilor corespunzătoare DCI-ului



Yüklə 4,39 Mb.
səhifə25/50
tarix25.07.2018
ölçüsü4,39 Mb.
#58042
1   ...   21   22   23   24   25   26   27   28   ...   50

Se aplică tuturor denumirilor comerciale, formelor farmaceutice şi concentraţiilor corespunzătoare DCI-ului.
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 18 Mui/0.6 ml

ROFERON A 18 Mui/0.6 ml ROCHE ROMANIA S.R.L.
L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 3 Mui/0.5 ml

ROFERON A 3 Mui/0.5 ml ROCHE ROMANIA S.R.L.


L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 4.5 Mui/0.5 ml

ROFERON A 4.5 Mui/0.5 ml ROCHE ROMANIA S.R.L.


L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 9 Mui/0.5 ml

ROFERON A 9 Mui/0.5 ml ROCHE ROMANIA S.R.L.


L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 3 Mui/0.5 ml

ROFERON A 3 Mui/0.5 ml ROCHE ROMANIA S.R.L.


L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 4.5 Mui/0.5 ml

ROFERON A 4.5 Mui/0.5 ml ROCHE ROMANIA S.R.L.


L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 9 Mui/0.5 ml

ROFERON A 9 Mui/0.5 ml ROCHE ROMANIA S.R.L.

________________________________________________________________________________
______________________________________________________________________________

| 398 |L03AB05| INTERFERONUM ALFA 2b**** | Protocol: J006N |

|_______|_______|____________________________________________|_________________|
Tratamentul cu interferon alfa a fost asociat cu depresie şi suicid la unii pacienţi. Pacienţii cu istoric de ideaţie suicidară sau boală depresivă trebuie avertizaţi de riscuri. Trebuie monitorizat statusul psihiatric în timpul tratamentului.

Se aplică tuturor denumirilor comerciale, formelor farmaceutice şi concentraţiilor corespunzătoare DCI-ului.
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

L03AB05 INTERFERONUM ALFA 2b SOL. INJ. PEN MULTIDOZĂ 18 milioane U.I.

INTRON A 18 milioane U.I. 18 milioane U.I. SP EUROPE
L03AB05 INTERFERONUM ALFA 2b SOL. INJ. PEN MULTIDOZĂ 30 milioane U.I.

INTRON A 30 milioane U.I. 30 milioane U.I. SP EUROPE

INTRON A 60 milioane U.I. 60 milioane U.I. SP EUROPE
L03AB05 INTERFERONUM ALFA 2b SOL. INJ. PEN MULTIDOZĂ 60 milioane U.I.

INTRON A 30 milioane U.I. 30 milioane U.I. SP EUROPE

INTRON A 60 milioane U.I. 60 milioane U.I. SP EUROPE

________________________________________________________________________________


______________________________________________________________________________

| 399 |L03AB10| PEGINTERFERON alfa-2b**** | Protocol: J003N |

|_______|_______|____________________________________________|_________________|
Tratamentul cu interferon alfa a fost asociat cu depresie şi suicid la unii pacienţi. Pacienţii cu istoric de ideaţie suicidară sau boală depresivă trebuie avertizaţi de riscuri. Trebuie monitorizat statusul psihiatric în timpul tratamentului.

Se aplică tuturor denumirilor comerciale, formelor farmaceutice şi concentraţiilor corespunzătoare DCI-ului.
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

L03AB10 PEGINTERFERON alfa-2b PULB. + SOLV. PT. SOL. 100 µg

INJ.

PEGINTRON 100 µg 100 µg SP EUROPE


L03AB10 PEGINTERFERON alfa-2b PULB. + SOLV. PT. SOL. 120 µg

INJ.


PEGINTRON 120 µg 120 µg SP EUROPE
L03AB10 PEGINTERFERON alfa-2b PULB. + SOLV. PT. SOL. 150 µg

INJ.


PEGINTRON 150 µg 150 µg SP EUROPE
L03AB10 PEGINTERFERON alfa-2b PULB. + SOLV. PT. SOL. 50 µg

INJ.


PEGINTRON 50 µg 50 µg SP EUROPE

________________________________________________________________________________


______________________________________________________________________________

| 400 |L03AB11| PEGINTERFERON alfa-2a**** | Protocol: J004N |

|_______|_______|____________________________________________|_________________|
Tratamentul cu interferon alfa a fost asociat cu depresie şi suicid la unii pacienţi. Pacienţii cu istoric de ideaţie suicidară sau boală depresivă trebuie avertizaţi de riscuri. Trebuie monitorizat statusul psihiatric în timpul tratamentului.

Se aplică tuturor denumirilor comerciale, formelor farmaceutice şi concentraţiilor corespunzătoare DCI-ului.
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

L03AB11 PEGINTERFERON alfa-2a SOL. INJ. 135 µg/ml

PEGASYS 135 µg/ml 135 µg/ml ROCHE REGISTRATION LTD.
L03AB11 PEGINTERFERON alfa-2a SOL. INJ. ÎN SERINGĂ 180 µg/0.5 ml

PREUMPLUTĂ

PEGASYS 180 µ/0,5 ml 180 µ/0.5 ml ROCHE REGISTRATION LTD.

________________________________________________________________________________


______________________________________________________________________________

| 401 |N04BB01| AMANTADINUM** | |

|_______|_______|____________________________________________|_________________|
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

N04BB01 AMANTADINUM CAPS. 100 mg

VIREGYT(R)-K 100 mg EGIS PHARMACEUTICALS LTD.

________________________________________________________________________________


SUBLISTA C1 - G5 HEPATITA AUTOIMUNĂ.
______________________________________________________________________________

| 402 |H02AB04| METHYLPREDNISOLONUM | |

|_______|_______|____________________________________________|_________________|
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

H02AB04 METHYLPREDNISOLONUM LIOF. PT. SOL. INJ. 125 mg

LEMOD SOLU 125 mg 125 mg HEMOFARM S.R.L
H02AB04 METHYLPREDNISOLONUM LIOF. ŞI SOLV. PT. 125 mg/2 ml

SOL. INJ.

SOLU - MEDROL ACT-O-VIAL 125 mg/2 ml PFIZER EUROPE MA EEIG
H02AB04 METHYLPREDNISOLONUM COMPR. 16 mg

MEDROL A 16 16 mg PFIZER EUROPE MA EEIG


H02AB04 METHYLPREDNISOLONUM LIOF. PT. SOL. INJ. 20 mg

LEMOD SOLU 20 mg 20 mg HEMOFARM S.R.L.


H02AB04 METHYLPREDNISOLONUM LIOF. ŞI SOLV. PT. 250 mg/4 ml

SOL. INJ.

SOLU - MEDROL ACT-O-VIAL 250 mg/4 ml PFIZER EUROPE MA EEIG
H02AB04 METHYLPREDNISOLONUM COMPR. 32 mg

MEDROL 32 32 mg PFIZER EUROPE MA EEIG


H02AB04 METHYLPREDNISOLONUM LIOF. PT. SOL. INJ. 40 mg

LEMOD SOLU 40 mg 40 mg HEMOFARM S.R.L.


H02AB04 METHYLPREDNISOLONUM LIOF. ŞI SOLV. PT. 40 mg/1 ml

SOL. INJ.

SOLU - MEDROL ACT-O-VIAL 40 mg/1 ml PFIZER EUROPE MA EEIG
H02AB04 METHYLPREDNISOLONUM COMPR. 4 mg

MEDROL 4 mg 4 mg PFIZER EUROPE MA EEIG


H02AB04 METHYLPREDNISOLONUM LIOF. PT. SOL. INJ. 500 mg

LEMOD SOLU 500 mg 500 mg HEMOFARM S.R.L.


H02AB04 METHYLPREDNISOLONUM LIOF. + SOLV. PT. SOL. 500 mg/7.8 ml

INJ.


SOLU - MEDROL 500 mg/7,8 ml 500 mg/7.8 ml PFIZER EUROPE MA EEIG

________________________________________________________________________________


______________________________________________________________________________

| 403 |H02AB06| PREDNISOLONUM | |

|_______|_______|____________________________________________|_________________|
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

H02AB06 PREDNISOLONUM LIOF. + SOLV. PT. SOL. 250 mg

INJ.

SOLU - DECORTIN H 250 250 mg MERCK KGAA


H02AB06 PREDNISOLONUM LIOF. + SOLV. PT. SOL. 50 mg

INJ.


SOLU - DECORTIN H 50 50 mg MERCK KGAA

________________________________________________________________________________


______________________________________________________________________________

| 404 |L04AX01| AZATHIOPRINUM* | |

|_______|_______|____________________________________________|_________________|
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

L04AX01 AZATHIOPRINUM COMPR. FILM. 50 mg

IMURAN(R) 50 mg THE WELLCOME FOUNDATION

LTD.


________________________________________________________________________________
SUBLISTA C1 - G06 CIROZA BILIARĂ PRIMARĂ, COLANGITA SCLEROZANTĂ PRIMITIVĂ, HEPATITA CRONICĂ ŞI CIROZE DE ALTE ETIOLOGII CU COLESTAZĂ.
______________________________________________________________________________

| 405 |A05AA02| ACIDUM URSODEOXYCHOLICUM | |

|_______|_______|____________________________________________|_________________|
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

A05AA02 ACIDUM CAPS. 300 mg

URSODEOXYCHOLICUM

URSOFALK(R) 250 mg DR. FALK PHARMA GMBH

URSOFALK(R) 250 mg DR. FALK PHARMA GMBH

URSOSAN 250 mg PRO. MED. CS PRAHA AS

________________________________________________________________________________
SUBLISTA C1 - G7 CIROZA HEPATICĂ.
______________________________________________________________________________

| 406 |A06AD11| LACTULOSUM* | |

|_______|_______|____________________________________________|_________________|
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

A06AD11 LACTULOSUM LICHID ORAL 66.7%

DUPHALAC(R) 66.7% SOLVAY PHARMACEUTICALS BV
A06AD11 LACTULOSUM

LACTULOSE AL SIROP 66.7% ALIUD PHARMA GMBH & CO.KG


A06AD11 LACTULOSUM

LAEVOLAC 670 mg/ml 670 mg/ml FRESENIUS KABI AUSTRIA

GMBH
A06AD11 LACTULOSUM SIROP 66.7%

LACTULOSE AL SIROP 66.7% ALIUD PHARMA GMBH & CO.KG


A06AD11 LACTULOSUM SOL. ORALĂ 670 mg/ml

LAEVOLAC 670 mg/ml 670 mg/ml FRESENIUS KABI AUSTRIA

GMBH
A06AD11 LACTULOSUM SIROP 66.7%

LACTULOSE AL SIROP 66.7% ALIUD PHARMA GMBH & CO.KG


A06AD11 LACTULOSUM SOL. ORALĂ 670 mg/ml

LAEVOLAC 670 mg/ml 670 mg/ml FRESENIUS KABI AUSTRIA

GMBH
A06AD11 LACTULOSUM LICHID ORAL 66.7%

DUPHALAC(R) 66.7% SOLVAY PHARMACEUTICALS BV


A06AD11 LACTULOSUM SIROP 65%

LACTULOSE 65% E.I.P.I.CO. MED S.R.L.

________________________________________________________________________________
______________________________________________________________________________

| 407 |A07AA11| RIFAXIMINUM* | |

|_______|_______|____________________________________________|_________________|
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

A07AA11 RIFAXIMINUM COMPR. FILM. 200 mg

NORMIX 200 mg 200 mg ALFA WASSERMANN SPA

________________________________________________________________________________


#M4

______________________________________________________________________________

| 408 | *** Abrogată |

|_______|______________________________________________________________________|
______________________________________________________________________________

| 409 | *** Abrogată |

|_______|______________________________________________________________________|
#B

______________________________________________________________________________

| 410 |C03CA01| FUROSEMIDUM | |

|_______|_______|____________________________________________|_________________|


Electroliţii serici trebuie să fie verificaţi periodic.

Se aplică tuturor denumirilor comerciale, formelor farmaceutice şi concentraţiilor corespunzătoare DCI-ului.
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

C03CA01 FUROSEMIDUM SOL. INJ. 10 mg/ml

FUROSEMID 20 mg/2 ml 10 mg/ml ZENTIVA SA
C03CA01 FUROSEMIDUM COMPR. 40 mg

FUROSEMID ARENA 40 mg 40 mg ARENA GROUP S.A.

FUROSEMID EEL 40 mg BIO EEL SRL

FUROSEMID LPH 40 mg 40 mg LABORMED PHARMA SA

FUROSEMID MCC 40 mg 40 mg MAGISTRA C & C SRL

FUROSEMID SLAVIA 40 mg SLAVIA PHARM SRL

FUROSEMID ZENTIVA 40 mg ZENTIVA SA

________________________________________________________________________________


______________________________________________________________________________

| 411 |C03DA01| SPIRONOLACTONUM | |

|_______|_______|____________________________________________|_________________|
Electroliţii serici trebuie să fie verificaţi periodic.

Femeile la vârsta fertilă la care s-a iniţiat tratament cu spironolactonă trebuie să ia măsuri adecvate de contracepţie.



Se aplică tuturor denumirilor comerciale, formelor farmaceutice şi concentraţiilor corespunzătoare DCI-ului.
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

C03DA01 SPIRONOLACTONUM CAPS. 100 mg

VEROSPIRON 100 mg GEDEON RICHTER LTD.
C03DA01 SPIRONOLACTONUM COMPR. 25 mg

SPIRONOLACTONA 25 mg 25 mg BIO EEL SRL


C03DA01 SPIRONOLACTONUM COMPR. FILM. 25 mg

ALSPIRON 25 mg 25 mg AC HELCOR PHARMA SRL

SPIRONOLACTONA 25 mg 25 mg TERAPIA SA
C03DA01 SPIRONOLACTONUM CAPS. 50 mg

VEROSPIRON 50 mg GEDEON RICHTER LTD.


C03DA01 SPIRONOLACTONUM COMPR. FILM. 50 mg

ALSPIRON 50 mg 50 mg AC HELCOR PHARMA SRL

________________________________________________________________________________
______________________________________________________________________________

| 412 |H02AB06| PREDNISOLONUM | |

|_______|_______|____________________________________________|_________________|
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

H02AB06 PREDNISOLONUM LIOF. + SOLV. PT. SOL. 250 mg

INJ.

SOLU - DECORTIN H 250 250 mg MERCK KGAA


H02AB06 PREDNISOLONUM LIOF. + SOLV. PT. SOL. 50 mg

INJ.


SOLU - DECORTIN H 50 50 mg MERCK KGAA

________________________________________________________________________________


______________________________________________________________________________

| 413 |J05AB04| RIBAVIRINUM**** | |

|_______|_______|____________________________________________|_________________|
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

J05AB04 RIBAVIRINUM CAPS. 200 mg

REBETOL 200 mg 200 mg SP EUROPE
J05AB04 RIBAVIRINUM COMPR. FILM. 200 mg

COPEGUS(R) 200 mg ROCHE ROMANIA SRL

________________________________________________________________________________
______________________________________________________________________________

| 414 |J05AF05| LAMIVUDINUM**** | |

|_______|_______|____________________________________________|_________________|
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

J05AF05 LAMIVUDINUM COMPR. FILM. 100 mg

ZEFFIX 100 mg 100 mg GLAXO GROUP LTD.
J05AF05 LAMIVUDINUM SOL. ORALĂ 10 mg/ml

EPIVIR 10 mg/ml 10 mg/ml GLAXO GROUP LTD.


J05AF05 LAMIVUDINUM COMPR. FILM. 150 mg

EPIVIR 150 mg 150 mg GLAXO GROUP LTD.


J05AF05 LAMIVUDINUM SOL. ORALĂ 5 mg/ml

ZEFFIX 5 mg/ml 5 mg/ml GLAXO GROUP LTD.

________________________________________________________________________________
______________________________________________________________________________

| 416 |J05AF10| ENTECAVIRUM**** | |

|_______|_______|____________________________________________|_________________|
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

J05AF10 ENTECAVIRUM COMPR. FILM. 0,5 mg

BARACLUDE 0,5 mg 0,5 mg BRISTOL-MYERS SQUIBB

PHARMA EEIG


J05AF10 ENTECAVIRUM COMPR. FILM. 1 mg

BARACLUDE 1 mg 1 mg BRISTOL-MYERS SQUIBB

PHARMA EEIG

________________________________________________________________________________


______________________________________________________________________________

| 417 |L03AA02| FILGRASTIMUM (G-CSF)** | Protocol: B013K |

|_______|_______|____________________________________________|_________________|
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

L03AA02 FILGRASTIMUM (G-CSF) SOL. INJ. 30 MU/0.5 ml

NEUPOGEN(R) 30 MU/0.5 ml AMGEN EUROPE B.V.
L03AA02 FILGRASTIMUM (G-CSF) SOL. INJ. 48 MU/0.5 ml

NEUPOGEN(R) 48 MU/0.5 ml AMGEN EUROPE B.V.

________________________________________________________________________________
______________________________________________________________________________

| 418 |L03AB04| INTERFERONUM ALFA 2a**** | |

|_______|_______|____________________________________________|_________________|
Tratamentul cu interferon alfa a fost asociat cu depresie şi suicid la unii pacienţi. Pacienţii cu istoric de ideaţie suicidară sau boală depresivă trebuie avertizaţi de riscuri. Trebuie monitorizat statusul psihiatric în timpul tratamentului.

Se aplică tuturor denumirilor comerciale, formelor farmaceutice şi concentraţiilor corespunzătoare DCI-ului.
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 18 Mui/0.6 ml

ROFERON A 18 Mui/0.6 ml ROCHE ROMANIA S.R.L.
L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 3 Mui/0.5 ml

ROFERON A 3 Mui/0.5 ml ROCHE ROMANIA S.R.L.


L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 4.5 Mui/0.5 ml

ROFERON A 4.5 Mui/0.5 ml ROCHE ROMANIA S.R.L.


L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 9 Mui/0.5 ml

ROFERON A 9 Mui/0.5 ml ROCHE ROMANIA S.R.L.


L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 3 Mui/0.5 ml

ROFERON A 3 Mui/0.5 ml ROCHE ROMANIA S.R.L.


L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 4.5 Mui/0.5 ml

ROFERON A 4.5 Mui/0.5 ml ROCHE ROMANIA S.R.L.


L03AB04 INTERFERONUM ALFA 2a SOL. INJ. 9 Mui/0.5 ml

ROFERON A 9 Mui/0.5 ml ROCHE ROMANIA S.R.L.

________________________________________________________________________________
______________________________________________________________________________

| 419 |L03AB05| INTERFERONUM ALFA 2b**** | |

|_______|_______|____________________________________________|_________________|
Tratamentul cu interferon alfa a fost asociat cu depresie şi suicid la unii pacienţi. Pacienţii cu istoric de ideaţie suicidară sau boală depresivă trebuie avertizaţi de riscuri. Trebuie monitorizat statusul psihiatric în timpul tratamentului.

Se aplică tuturor denumirilor comerciale, formelor farmaceutice şi concentraţiilor corespunzătoare DCI-ului.
________________________________________________________________________________

DCI/DENUMIRE COMERCIALĂ FORMA FARM.

__________________________________________________

CONCENTRAŢIE FIRMA

________________________________________________________________________________

L03AB05 INTERFERONUM ALFA 2b SOL. INJ. PEN MULTIDOZĂ 18 milioane U.I.

INTRON A 18 milioane U.I. 18 milioane U.I. SP EUROPE
L03AB05 INTERFERONUM ALFA 2b SOL. INJ. PEN MULTIDOZĂ 30 milioane U.I.

INTRON A 30 milioane U.I. 30 milioane U.I. SP EUROPE

INTRON A 60 milioane U.I. 60 milioane U.I. SP EUROPE
L03AB05 INTERFERONUM ALFA 2b SOL. INJ. PEN MULTIDOZĂ 60 milioane U.I.

INTRON A 30 milioane U.I. 30 milioane U.I. SP EUROPE

INTRON A 60 milioane U.I. 60 milioane U.I. SP EUROPE

________________________________________________________________________________


______________________________________________________________________________

| 420 |L03AB10| PEGINTERFERON alfa-2b**** | |

|_______|_______|____________________________________________|_________________|
Tratamentul cu interferon alfa a fost asociat cu depresie şi suicid la unii pacienţi. Pacienţii cu istoric de ideaţie suicidară sau boală depresivă trebuie avertizaţi de riscuri. Trebuie monitorizat statusul psihiatric în timpul tratamentului.


Yüklə 4,39 Mb.

Dostları ilə paylaş:
1   ...   21   22   23   24   25   26   27   28   ...   50




Verilənlər bazası müəlliflik hüququ ilə müdafiə olunur ©muhaz.org 2024
rəhbərliyinə müraciət

gir | qeydiyyatdan keç
    Ana səhifə


yükləyin