# Nifedipine

NDC: 55289-798
Generic name: Nifedipine
Labeler / Manufacturer: PD-Rx Pharmaceuticals, 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: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55289-798"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55289-798
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=86c1bdae-c749-4ec3-90f6-7ebe8e76c461