FDA NDC Directory · JSON-LD · Markdown

Acetazolamide

NDC 68083-661 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA219775
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsACETAZOLAMIDE SODIUM (500 mg/5mL)
Marketing started20250617
Package count1

External sources

Source: openFDA. Public-domain (CC0).