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Tolmetin Sodium

NDC 71993-312 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAtland Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074473
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOLMETIN SODIUM (600 mg/1)
Marketing started20250225
Package count1

External sources

Source: openFDA. Public-domain (CC0).