Active Ingredient: KANAMYCIN SULFATE
Proprietary Name: KANTREX
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 500MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A061911
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: APOTHECON INC DIV BRISTOL MYERS SQUIBB
Marketing Status:
Discontinued
Patent and Exclusivity Information