acetazolamide
- Product NDC
- 23155-120
- 11-digit product format
- 231550120
- Labeler code
- 23155
- Product ID
- 23155-120_ee8a2c2d-1b1a-4a2b-bf05-8e63868a7e54
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acetazolamide
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Application
- ANDA090779
- Marketing category
- ANDA
- Marketing start
- 2012-09-24
- Marketing end
- 2022-12-31
- Substance
- ACETAZOLAMIDE
- Active strength
- 500 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
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 23155-120-01 | 23155012001 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (23155-120-01) | 2012-09-24 | 0000-00-00 | No | No | Current |
| 23155-120-05 | 23155012005 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (23155-120-05) | 2012-09-24 | 0000-00-00 | No | No | Current |