Alprazolam
- Product NDC
- 49999-252
- 11-digit product format
- 499990252
- Labeler code
- 49999
- Product ID
- 49999-252_d9bb7212-1075-4735-ae43-5c9107528463
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products LLC
- Application
- NDA018276
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2011-11-15
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49999-252-30 | 49999025230 | 30 TABLET in 1 BOTTLE (49999-252-30) | 30 tablet | 2021-12-03 | 0000-00-00 | No | No | Current |