Active Ingredient: NIFEDIPINE
Proprietary Name: NIFEDIPINE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 90MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB2
Application Number: A212016
Product Number: 001
Approval Date: Nov 18, 2020
Applicant Holder Full Name: ELITE PHARMACEUTICAL SOLUTION INC
Marketing Status:
Prescription
Patent and Exclusivity Information