Active Ingredient: NIFEDIPINE
Proprietary Name: NIFEDIPINE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 30MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077899
Product Number: 001
Approval Date: Dec 13, 2006
Applicant Holder Full Name: PAR PHARMACEUTICAL INC
Marketing Status:
Discontinued
Patent and Exclusivity Information