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Norepinephrine Bitartrate

NDC 71288-439 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Labeler / ManufacturerMeitheal Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040455
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsNOREPINEPHRINE BITARTRATE (1 mg/mL)
Marketing started20241201
Package count1

External sources

Source: openFDA. Public-domain (CC0).