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Acetazolamide

NDC 46708-349 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA210423
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsACETAZOLAMIDE (500 mg/1)
Marketing started20190220
Package count2

External sources

Source: openFDA. Public-domain (CC0).