# TOLMETIN SODIUM

NDC: 16571-825
Generic name: tolmetin sodium
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230411
Marketing ended: 20260531
FDA application: ANDA074473

## Active ingredients

- TOLMETIN SODIUM: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16571-825"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-825
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fa4096f0-0d22-4421-b4ca-6b1d7f078bd3