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Active Ingredient: NIFEDIPINE
Proprietary Name: NIFEDIPINE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A072556
Product Number: 001
Approval Date: Sep 20, 1990
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
