# NATEGLINIDE

NDC: 16571-758
Generic name: NATEGLINIDE
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201216

FDA application: ANDA205544

## 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:"16571-758"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-758
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b41f4180-96a7-411d-b827-5021e534f556