Active Ingredient: KANAMYCIN SULFATE
Proprietary Name: KANAMYCIN SULFATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/3ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A063092
Product Number: 001
Approval Date: Oct 11, 1989
Applicant Holder Full Name: WARNER CHILCOTT DIV WARNER LAMBERT CO
Marketing Status:
Discontinued
Patent and Exclusivity Information