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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 210434

ALBENDAZOLE (ALBENDAZOLE)
200MG
Marketing Status: Discontinued
Active Ingredient: ALBENDAZOLE
Proprietary Name: ALBENDAZOLE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A210434
Product Number: 001
Approval Date: Sep 21, 2018
Applicant Holder Full Name: CIPLA LTD
Marketing Status:  Discontinued
Patent and Exclusivity Information
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