# Tolmetin Sodium

NDC: 16571-826
Generic name: Tolmetin Sodium
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20230630
Marketing ended: 20260531
FDA application: ANDA073393

## Active ingredients

- TOLMETIN SODIUM: 400 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16571-826"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-826
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=740a0f37-aa95-4558-b415-be516b8c40a3