Alprazolam
- Product NDC
- 63629-8164
- 11-digit product format
- 636298164
- Labeler code
- 63629
- Product ID
- 63629-8164_01cefc76-f93f-44a5-b9a8-bea21ee587a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074174
- Marketing category
- ANDA
- Marketing start
- 2007-03-28
- 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
- 2020-12-31
- 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 |
|---|
| 63629-8164-1 | 63629816401 | 30 TABLET in 1 BOTTLE (63629-8164-1) | 30 tablet | 2019-07-03 | 0000-00-00 | No | No | Current |