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Methimazole

NDC 0832-6072 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerUpsher-Smith Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040547
Dosage form / routeTABLET · ORAL
Active ingredientsMETHIMAZOLE (5 mg/1)
Marketing started20160701
Package count1

External sources

Source: openFDA. Public-domain (CC0).