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Diethylpropion Hydrochloride

NDC 0527-1475 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200177
Dosage form / routeTABLET · ORAL
Active ingredientsDIETHYLPROPION HYDROCHLORIDE (25 mg/1)
Marketing started20110718
Package count1

External sources

Source: openFDA. Public-domain (CC0).