Orange Book product · Generic (ANDA)
CIMETIDINE HYDROCHLORIDE
CIMETIDINE HYDROCHLORIDE
At a glance
Sep 26, 1996
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 26, 1996
30 yr 2 mo ago
Today
Pharmaceutical detail
Active ingredient
CIMETIDINE HYDROCHLORIDE
Strength
EQ 300MG BASE/5ML
Dosage form
SOLUTION
Route
ORAL
TE code
Not listed
Application
ANDA 074610
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of CIMETIDINE HYDROCHLORIDE
- 1985TAGAMET HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINERBrand (NDA)
NDA 019434 · GLAXOSMITHKLINE
- —TAGAMETBrand (NDA)
NDA 017939 · GLAXOSMITHKLINE
- —TAGAMETBrand (NDA)
NDA 017924 · GLAXOSMITHKLINE
- 2000CIMETIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 075560 · PHARM ASSOC
- 1998CIMETIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 074859 · ANI PHARMS
- 1998CIMETIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 075110 · ANI PHARMS
- 1997CIMETIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 074252 · TEVA PARENTERAL
- 1997CIMETIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 074664 · PAI HOLDINGS PHARM
- 1997CIMETIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 074757 · PHARMOBEDIENT CNSLTG
- 1997CIMETIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 074541 · CYCLE
- 1997CIMETIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 074296 · HOSPIRA
- 1997CIMETIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 074412 · HOSPIRA
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.

