Active Ingredient: GENTAMICIN SULFATE
Proprietary Name: GENTAMICIN SULFATE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: EQ 0.3% BASE
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AT
Application Number: A062196
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Prescription
Patent and Exclusivity Information
