# NIFEDIPINE

NDC: 69315-212
Generic name: NIFEDIPINE
Labeler / Manufacturer: Leading Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20161123

FDA application: ANDA074045

## Active ingredients

- NIFEDIPINE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69315-212"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69315-212
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fd5d3311-f46d-4376-a4c1-bd8fa0eac057