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Scopolamine

NDC 70710-1846 · HUMAN PRESCRIPTION DRUG · PATCH, EXTENDED RELEASE

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217893
Dosage form / routePATCH, EXTENDED RELEASE · TRANSDERMAL
Active ingredientsSCOPOLAMINE (1 mg/3d)
Marketing started20240905
Package count3

External sources

Source: openFDA. Public-domain (CC0).