# Nifedipine

NDC: 62175-261
Generic name: Nifedipine
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20051121

FDA application: ANDA077127

## 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:"62175-261"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62175-261
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=331db003-cc8e-4509-9415-20e48c5cc5b2