Active Ingredient: GUANETHIDINE MONOSULFATE
Proprietary Name: ISMELIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 10MG SULFATE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N012329
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information
