Acetazolamide
- Product NDC
- 50090-0279
- 11-digit product format
- 500900279
- Labeler code
- 50090
- Product ID
- 50090-0279_b08268cc-cf9b-444d-b3bd-199663e79a96
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetazolamide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040195
- Marketing category
- ANDA
- Marketing start
- 1997-05-28
- Marketing end
- 0000-00-00
- Substance
- ACETAZOLAMIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA],Sulfonamides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record