Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 074488

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RANITIDINE HYDROCHLORIDE (RANITIDINE HYDROCHLORIDE)
EQ 150MG BASE
Marketing Status: Discontinued

Active Ingredient: RANITIDINE HYDROCHLORIDE
Proprietary Name: RANITIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 150MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A074488
Product Number: 001
Approval Date: Jul 31, 1997
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

RANITIDINE HYDROCHLORIDE (RANITIDINE HYDROCHLORIDE)
EQ 300MG BASE
Marketing Status: Discontinued

Active Ingredient: RANITIDINE HYDROCHLORIDE
Proprietary Name: RANITIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 300MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A074488
Product Number: 002
Approval Date: Jul 31, 1997
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information