# nifedipine

NDC: 70807-503
Generic name: nifedipine
Labeler / Manufacturer: Elite Pharmaceutical Solution, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20211015

FDA application: ANDA212016

## Active ingredients

- NIFEDIPINE: 90 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70807-503"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70807-503
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1df07edb-630d-4c70-a68c-bdbc607ce850