Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 065161

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AMOXICILLIN AND CLAVULANATE POTASSIUM (AMOXICILLIN; CLAVULANATE POTASSIUM)
200MG;EQ 28.5MG BASE
Marketing Status: Discontinued

Active Ingredient: AMOXICILLIN; CLAVULANATE POTASSIUM
Proprietary Name: AMOXICILLIN AND CLAVULANATE POTASSIUM
Dosage Form; Route of Administration: TABLET, CHEWABLE; ORAL
Strength: 200MG;EQ 28.5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A065161
Product Number: 001
Approval Date: Dec 3, 2003
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:  Discontinued
Patent and Exclusivity Information

AMOXICILLIN AND CLAVULANATE POTASSIUM (AMOXICILLIN; CLAVULANATE POTASSIUM)
400MG;EQ 57MG BASE
Marketing Status: Discontinued

Active Ingredient: AMOXICILLIN; CLAVULANATE POTASSIUM
Proprietary Name: AMOXICILLIN AND CLAVULANATE POTASSIUM
Dosage Form; Route of Administration: TABLET, CHEWABLE; ORAL
Strength: 400MG;EQ 57MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A065161
Product Number: 002
Approval Date: Dec 3, 2003
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:  Discontinued
Patent and Exclusivity Information