Alprazolam
- Product NDC
- 68788-9682
- 11-digit product format
- 687889682
- Labeler code
- 68788
- Product ID
- 68788-9682_8c804e62-2699-4067-a5c4-fb917f853694
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA090871
- Marketing category
- ANDA
- Marketing start
- 2013-04-22
- 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 |
|---|
| 68788-9682-3 | 68788968203 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9682-3) | 2013-04-22 | 0000-00-00 | No | No | Current |
| 68788-9682-6 | 68788968206 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9682-6) | 2013-04-22 | 0000-00-00 | No | No | Current |
| 68788-9682-9 | 68788968209 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9682-9) | 2013-04-22 | 0000-00-00 | No | No | Current |