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METHSCOPOLAMINE BROMIDE

NDC 72319-030 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namemethscopolamine bromide
Labeler / Manufactureri3 Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216786
Dosage form / routeTABLET · ORAL
Active ingredientsMETHSCOPOLAMINE BROMIDE (5 mg/1)
Marketing started20241218
Package count2

External sources

Source: openFDA. Public-domain (CC0).