# Nateglinide

NDC: 72241-003
Generic name: Nateglinide
Labeler / Manufacturer: Modavar Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20210819

FDA application: ANDA206432

## Active ingredients

- NATEGLINIDE: 120 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72241-003"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72241-003
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=af81465b-5f49-4eeb-8122-ef7fe5d90ddc