Active Ingredient: MINOCYCLINE HYDROCHLORIDE
Proprietary Name: MINOCIN
Dosage Form; Route of Administration: SUSPENSION; ORAL
Strength: EQ 50MG BASE/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050445
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BAUSCH HEALTH US LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information