Active Ingredient: GUANIDINE HYDROCHLORIDE
Proprietary Name: GUANIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 125MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N001546
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MERCK SHARP AND DOHME CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information
