Alprazolam
- Product NDC
- 70518-3259
- 11-digit product format
- 705183259
- Labeler code
- 70518
- Product ID
- 70518-3259_cfbabe61-a7b2-5385-e053-2995a90aa9c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074342
- Marketing category
- ANDA
- Marketing start
- 2021-10-29
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3259 | ALPRAZOLAM TABLET [REMEDYREPACK INC.] | 3 | Legacy NDC | 20240316_5fe0fa45-f959-4dc7-a0c4-594ee8e66e9b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3259-0 | 70518325900 | 60 TABLET in 1 BOTTLE, PLASTIC (70518-3259-0) | 60 tablet | 2021-10-29 | 0000-00-00 | No | No | Current |