AcetaZOLAMIDE
- Product NDC
- 68084-541
- 11-digit product format
- 680840541
- Labeler code
- 68084
- Product ID
- 68084-541_de5910df-0668-deee-e053-2a95a90a7490
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetazolamide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA084840
- Marketing category
- ANDA
- Marketing start
- 2011-12-28
- Marketing end
- 2022-10-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68084-541-01 | 68084054101 | 10 BLISTER PACK in 1 CARTON (68084-541-01) > 10 TABLET in 1 BLISTER PACK (68084-541-11) | 10 blister pack | 2011-12-28 | 0000-00-00 | No | No | Current |