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Active Ingredient: RANITIDINE HYDROCHLORIDE
Proprietary Name: RANITIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 75MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A075296
Product Number: 001
Approval Date: Jan 14, 2000
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information