# Nateglinide

NDC: 60687-673
Generic name: nateglinide
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230112

FDA application: ANDA077463

## Active ingredients

- NATEGLINIDE: 60 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-673"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-673
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b17ead66-dc11-4e54-9ba6-00619510f27b