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Atropine Sulfate

NDC 0404-9802 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHenry Schein, Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA216120
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsATROPINE SULFATE (.4 mg/mL)
Marketing started20240822
Package count1

External sources

Source: openFDA. Public-domain (CC0).