Active Ingredient: MINOCYCLINE HYDROCHLORIDE
Proprietary Name: MINOCIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 100MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A062139
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: LEDERLE LABORATORIES DIV AMERICAN CYANAMID CO
Marketing Status:
Discontinued
Patent and Exclusivity Information