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Active Ingredient: CIMETIDINE HYDROCHLORIDE
Proprietary Name: CIMETIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: EQ 300MG BASE/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A074176
Product Number: 001
Approval Date: Jun 1, 1994
Applicant Holder Full Name: G AND W LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information