# Tolmetin Sodium

NDC: 71993-312
Generic name: Tolmetin Sodium
Labeler / Manufacturer: Atland Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250225

FDA application: ANDA074473

## Active ingredients

- TOLMETIN SODIUM: 600 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71993-312"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71993-312
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e6150446-c5ef-4437-b488-067876649fcc