Active Ingredient: AMOXICILLIN
Proprietary Name: AMOXICILLIN
Dosage Form; Route of Administration: TABLET, CHEWABLE; ORAL
Strength: 125MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A065021
Product Number: 001
Approval Date: Dec 23, 1999
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information