Active Ingredient: MINOCYCLINE HYDROCHLORIDE
Proprietary Name: MINOCIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 100MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N050444
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: REMPEX PHARMACEUTICALS INC A WHOLLY OWNED SUB OF MELINTA THERAPEUTICS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
