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Glucagon

NDC 63323-596 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryNew Drug Application (innovator) · App NDA201849
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsGLUCAGON HYDROCHLORIDE (1 mg/mL)
Marketing started20150508
Package count1

External sources

Source: openFDA. Public-domain (CC0).