# Nifedipine

NDC: 50742-261
Generic name: nifedipine
Labeler / Manufacturer: Ingenus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20190312

FDA application: ANDA210614

## Active ingredients

- NIFEDIPINE: 60 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50742-261"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-261
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d3e11d2-d320-45d3-96c8-48322202b504