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Tolmetin Sodium

NDC 72336-118 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLifsa Drugs LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA073588
Dosage form / routeTABLET · ORAL
Active ingredientsTOLMETIN SODIUM (200 mg/1)
Marketing started19920731
Package count1

External sources

Source: openFDA. Public-domain (CC0).