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Product Details for ANDA 202941

LAMIVUDINE (LAMIVUDINE)
100MG
Marketing Status: Prescription
Active Ingredient: LAMIVUDINE
Proprietary Name: LAMIVUDINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A202941
Product Number: 001
Approval Date: Jan 2, 2014
Applicant Holder Full Name: APOTEX INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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