# Nifedipine

NDC: 71205-965
Generic name: Nifedipine
Labeler / Manufacturer: Proficient Rx LP
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:"71205-965"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-965
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d428aa4d-4cc0-4b1e-b9f6-40ae65a735d6
