Alprazolam
- Product NDC
- 68071-2236
- 11-digit product format
- 680712236
- Labeler code
- 68071
- Product ID
- 68071-2236_ee27dfb4-1ede-eb54-e053-2995a90ab1de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA207507
- Marketing category
- ANDA
- Marketing start
- 2018-07-09
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 0 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2236 | ALPRAZOLAM TABLET [NUCARE PHARMACEUTICALS,INC.] | 4 | Legacy NDC | 20240820_acb0f6b4-b020-aa93-e053-2995a90a9aee.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2236-6 | 68071223606 | 6 TABLET in 1 BOTTLE (68071-2236-6) | 6 tablet | 2020-08-12 | 0000-00-00 | No | No | Current |