AcetaZOLAMIDE
- Product NDC
- 42291-103
- 11-digit product format
- 422910103
- Labeler code
- 42291
- Product ID
- 42291-103_d5794985-97ab-3b24-e053-2a95a90a5a92
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetazolamide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA084840
- Marketing category
- ANDA
- Marketing start
- 2012-07-02
- 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
- 2023-12-31
- 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 |
|---|
| 42291-103-10 | 42291010310 | 1000 TABLET in 1 BOTTLE (42291-103-10) | 1000 tablet | 2013-09-10 | 0000-00-00 | No | No | Current |