Acetazolamide
- Product NDC
- 71335-1370
- 11-digit product format
- 713351370
- Labeler code
- 71335
- Product ID
- 71335-1370_0175f100-4cdf-4b31-83e9-356e14754db3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetazolamide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209734
- Marketing category
- ANDA
- Marketing start
- 2017-11-20
- 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 |
|---|
| 71335-1370-1 | 71335137001 | 30 TABLET in 1 BOTTLE (71335-1370-1) | 30 tablet | 2020-11-24 | 0000-00-00 | No | No | Current |
| 71335-1370-2 | 71335137002 | 60 TABLET in 1 BOTTLE (71335-1370-2) | 60 tablet | 2021-02-11 | 0000-00-00 | No | No | Current |
| 71335-1370-3 | 71335137003 | 6 TABLET in 1 BOTTLE (71335-1370-3) | 6 tablet | 2022-09-28 | 0000-00-00 | No | No | Current |
| 71335-1370-4 | 71335137004 | 180 TABLET in 1 BOTTLE (71335-1370-4) | 180 tablet | 2019-10-17 | 0000-00-00 | No | No | Current |