Alprazolam
- Product NDC
- 63629-5364
- 11-digit product format
- 636295364
- Labeler code
- 63629
- Product ID
- 63629-5364_7e96bc50-4985-4c19-8be9-4f4cf7184c64
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078056
- Marketing category
- ANDA
- Marketing start
- 2007-03-12
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-5364-1 | 63629536401 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-5364-1) | 2016-06-21 | 0000-00-00 | No | No | Current |
| 63629-5364-2 | 63629536402 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-5364-2) | 2014-06-16 | 0000-00-00 | No | No | Current |
| 63629-5364-3 | 63629536403 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-5364-3) | 2016-06-20 | 0000-00-00 | No | No | Current |
| 63629-5364-4 | 63629536404 | 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-5364-4) | 2022-02-08 | 0000-00-00 | No | No | Current |