# Nifedipine

NDC: 62135-740
Generic name: Nifedipine
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20101207

FDA application: ANDA202644

## 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:"62135-740"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-740
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5014847e-389d-48c1-8350-b9b24ca8d2a4