FDA NDC Directory · JSON-LD · Markdown

NEOSTIGMINE METHYLSULFATE

NDC 0548-9601 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameneostigmine methylsulfate
Labeler / ManufacturerAmphastar Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209933
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsNEOSTIGMINE METHYLSULFATE (.5 mg/mL)
Marketing started20170925
Package count1

External sources

Source: openFDA. Public-domain (CC0).