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Scopolamine

NDC 42858-150 · HUMAN PRESCRIPTION DRUG · PATCH, EXTENDED RELEASE

Labeler / ManufacturerRhodes Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215329
Dosage form / routePATCH, EXTENDED RELEASE · TRANSDERMAL
Active ingredientsSCOPOLAMINE (1 mg/3d)
Marketing started20241101
Package count3

External sources

Source: openFDA. Public-domain (CC0).