Active Ingredient: VANCOMYCIN HYDROCHLORIDE
Proprietary Name: VANCOCIN HYDROCHLORIDE
Dosage Form; Route of Administration: FOR SOLUTION; ORAL
Strength: EQ 500MG BASE/6ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A061667
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information