# Nifedipine

NDC: 71335-9651
Generic name: Nifedipine
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20141101

FDA application: ANDA203126

## Active ingredients

- NIFEDIPINE: 90 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-9651"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-9651
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6a68f67f-5b68-4f83-aad8-fc3177f5a0a4