acetazolamide
- Product NDC
- 63629-7889
- 11-digit product format
- 636297889
- Labeler code
- 63629
- Product ID
- 63629-7889_167dc570-2b36-4161-9abf-0915f339c9bf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acetazolamide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205530
- Marketing category
- ANDA
- Marketing start
- 2016-10-27
- 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 |
|---|
| 63629-7889-1 | 63629788901 | 30 TABLET in 1 BOTTLE (63629-7889-1) | 30 tablet | 2022-04-29 | 0000-00-00 | No | No | Current |
| 63629-7889-2 | 63629788902 | 60 TABLET in 1 BOTTLE (63629-7889-2) | 60 tablet | 2019-01-08 | 0000-00-00 | No | No | Current |
| 63629-7889-3 | 63629788903 | 6 TABLET in 1 BOTTLE (63629-7889-3) | 6 tablet | 2022-04-29 | 0000-00-00 | No | No | Current |
| 63629-7889-4 | 63629788904 | 180 TABLET in 1 BOTTLE (63629-7889-4) | 180 tablet | 2022-04-29 | 0000-00-00 | No | No | Current |