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RANITIDINE HYDROCHLORIDE

ANDA

RANITIDINE HYDROCHLORIDE | A075180 | PH HEALTH LTD

2 strengths0 unique patents0 unique exclusivities

API Supply Chain4 active DMFs30 inactive

3 active API suppliers hold Drug Master Files for this ingredient.

DR REDDYS LABORATORIES LTDRANITIDINE HYDROCHLORIDE (FORM I)

DMF 121661996

DR REDDYS LABORATORIES LTDRANITIDINE HYDROCHLORIDE [FORM-2]

DMF 201272007

ORCHEV PHARMA PVT LTDRANITIDINE HYDROCHLORIDE USP

DMF 258512012

SMS PHARMACEUTICALS LTDRANITIDINE HYDROCHLORIDE USP (PROCESS -2)

DMF 315752017

SHANGHAI NO 6 PHARMACEUTICAL FACTORYInactiveRANITIDINE HYDROCHLORIDE

DMF 75281988

QUIMICA SINTETICA SAInactiveRANITIDINE HYDROCHLORIDE

DMF 84941990

PHARMAGLOBE LABORATORIES LTDInactiveRANITIDINE HYDROCHLORIDE

DMF 89531991

FIRST SOUTHWEST PHARMACEUTICAL FACTORYInactiveRANITIDINE

DMF 90801991

UNION QUIMICO FARMACEUTICA SA (UQUIFA SA)InactiveRANITIDINE HYDROCHLORIDE (CRYSTALLINE FORM 1)

DMF 102731993

RANBAXY LABORATORIES LTDInactiveRANITIDINE HYDROCHLORIDE

DMF 105161993

CHEMICAL PHARMACEUTICAL RESEARCH INSTITUTE NIHFI LTDInactiveRANITIDINE HYDROCHLORIDE

DMF 106821993

NOVOPHARM LTDInactiveRANITIDINE HYDROCHLORIDE USP

DMF 108851994

BOEHRINGER INGELHEIM CHEMICALS INCInactiveRANITIDINE HYDROCHLORIDE USP

DMF 114801995

MAPRIMED SAInactiveRANITIDINE HYDROCHLORIDE

DMF 115431995

DR REDDYS LABORATORIES LTDInactiveRANITIDINE

DMF 115461995

HOECHST MARION ROUSSEL INCInactiveRANITIDINE HYDROCHLORIDE USP, FORM 1

DMF 118241996

GENPHARM INCInactiveRANITIDINE HYDROCHLORIDE USP FORM 1

DMF 118391996

SUN PHARMACEUTICAL INDUSTRIES LTDInactiveRANITIDINE HYDROCHLORIDE USP

DMF 122071996

NEULAND LABORATORIES LTDInactiveRANITIDINE

DMF 125031997

NEULAND LABORATORIES LTDInactiveRANITIDINE HYDROCHLORIDE (FORM I)

DMF 125321997

SOLARA ACTIVE PHARMA SCIENCES LTDInactiveRANITIDINE

DMF 125431997

WOCKHARDT LTDInactiveRANITIDINE HYDROCHLORIDE

DMF 125521997

SHASUN CHEMICALS AND DRUGS LTDInactiveRANITIDINE HYDROCHLORIDE

DMF 126651997

FAKO ILACLARI ASInactiveRANITIDINE HYDROCHLORIDE FORM I BULK

DMF 144151999

SOLARA ACTIVE PHARMA SCIENCES LTDInactiveRANITIDINE HYDROCHLORIDE

DMF 144681999

FAKO ILACLARI ASInactiveRANITIDINE HYDROCHLORIDE FORM I BULK

DMF 151252000

NEULAND LABORATORIES LTDInactiveRANITIDINE HYDROCHLORIDE USP

DMF 151412000

FARCHEMIA SRLInactiveRANITIDINE HYDROCHLORIDE

DMF 156762001

FAKO ILACLARI ASInactiveRANITIDINE HYDROCHLORIDE FORM II

DMF 159942002

SMS PHARMACEUTICALS LTDInactiveRANITIDINE HYDROCHLORIDE

DMF 175422004

SARACA LABORATORIES LTDInactiveRANITIDINE HYDROCHLORIDE (FORM-II)

DMF 176982004

SMS PHARMACEUTICALS LTDInactiveRANITIDINE HYDROCHLORIDE USP

DMF 181292005

WOCKHARDT LTDInactiveRANITIDINE HYDROCHLORIDE USP (FORM II)

DMF 195002006

SMS PHARMACEUTICALS LTDInactiveRANITIDINE HYDROCHLORIDE USP (UNIT-VII)

DMF 256082011

Source: FDA Drug Master Files (fda.gov). Type II API DMFs matched by ingredient.

Approval Letters

1 letter from Drugs@FDA

Date	Submission	Document
Jan 28, 1999	ORIG -1	View Letter (PDF)

Source: Drugs@FDA application documents.

Products (2)

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#001 — EQ 150MG BASE

0 patents0 exclusivities▴

TABLET;ORAL | Approved: Jan 28, 1999

No patent or exclusivity listings for this strength.

#002 — EQ 300MG BASE

0 patents0 exclusivities▾

TABLET;ORAL | Approved: Jan 28, 1999