Composition
- Active ingredients
- ACETAZOLAMIDE 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- ACETAZOLAMIDE 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA008943-002 · Discontinued
- ACETAZOLAMIDE 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA008943-001 · Discontinued
- ACETAZOLAMIDE 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Capsule, extended releaseThis page
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA012945.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Diamox
- Active substance
- acetazolamide
- Route
- Oral
- Dosage form
- Capsule, extended release
- Applicant
- Teva Branded Pharm
- Status
- Discontinued
- FDA approval
- 25 Jan 1962
- Application
- NDA012945-001



