Alprazolam
- Product NDC
- 68788-6943
- 11-digit product format
- 687886943
- Labeler code
- 68788
- Product ID
- 68788-6943_c8dac777-b196-465e-851e-8a583c2ae784
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078056
- Marketing category
- ANDA
- Marketing start
- 2017-04-14
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-6943-3 | 68788694303 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-6943-3) | 2017-04-14 | 0000-00-00 | No | No | Current |
| 68788-6943-6 | 68788694306 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-6943-6) | 2017-04-14 | 0000-00-00 | No | No | Current |
| 68788-6943-9 | 68788694309 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-6943-9) | 2017-04-14 | 0000-00-00 | No | No | Current |