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Glycopyrrolate

NDC 0781-3831 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerSandoz Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA211334
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsGLYCOPYRROLATE (4 mg/20mL)
Marketing started20190722
Package count1

External sources

Source: openFDA. Public-domain (CC0).