Acetazolamide
- Product NDC
- 63629-8257
- 11-digit product format
- 636298257
- Labeler code
- 63629
- Product ID
- 63629-8257_1dd4520e-3a89-4b65-8645-ed321a2e945f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetazolamide
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204691
- Marketing category
- ANDA
- Marketing start
- 2016-03-30
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8257-1 | 63629825701 | 180 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-8257-1) | 2019-10-21 | 0000-00-00 | No | No | Current |