# Tolmetin Sodium

NDC: 72336-118
Generic name: Tolmetin Sodium
Labeler / Manufacturer: Lifsa Drugs LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19920731

FDA application: ANDA073588

## Active ingredients

- TOLMETIN SODIUM: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72336-118"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72336-118
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7b26321c-4797-4664-a162-e29de4b8dd93