# Nifedipine

NDC: 72789-484
Generic name: Nifedipine
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220330

FDA application: ANDA216067

## 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:"72789-484"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-484
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=89723620-474e-4b16-9f57-4e927efc401c