Active Ingredient: NIFEDIPINE
Proprietary Name: NIFEDIPINE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A072781
Product Number: 001
Approval Date: Jul 30, 1993
Applicant Holder Full Name: ACELLA PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information