Alprazolam
- Product NDC
- 68071-5128
- 11-digit product format
- 680715128
- Labeler code
- 68071
- Product ID
- 68071-5128_e8048c65-018a-11db-e053-2a95a90a8097
- 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
- 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-5128 | ALPRAZOLAM TABLET [NUCARE PHARMACEUTICALS,INC.] | 5 | Legacy NDC | 20240623_99757bac-7836-f62e-e053-2995a90a9f6c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-5128-3 | 68071512803 | 30 TABLET in 1 BOTTLE (68071-5128-3) | 30 tablet | 2019-12-11 | 0000-00-00 | No | No | Current |
| 68071-5128-9 | 68071512809 | 90 TABLET in 1 BOTTLE (68071-5128-9) | 90 tablet | 2019-12-11 | 0000-00-00 | No | No | Current |