Alprazolam
- Product NDC
- 35356-744
- 11-digit product format
- 353560744
- Labeler code
- 35356
- Product ID
- 35356-744_47476b37-3331-4402-b370-48b50a2e5eb3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
- Application
- ANDA074112
- Marketing category
- ANDA
- Marketing start
- 1995-12-29
- 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
- 2022-12-31
- 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 |
|---|
| 35356-744-30 | 35356074430 | 30 TABLET in 1 BOTTLE (35356-744-30) | 30 tablet | 2011-11-01 | 0000-00-00 | No | No | Current |
| 35356-744-60 | 35356074460 | 60 TABLET in 1 BOTTLE (35356-744-60) | 60 tablet | 2021-04-22 | 0000-00-00 | No | No | Current |