Alprazolam
- Product NDC
- 51655-266
- 11-digit product format
- 516550266
- Labeler code
- 51655
- Product ID
- 51655-266_d4790a90-436a-bd13-e053-2a95a90a4eb5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA207507
- Marketing category
- ANDA
- Marketing start
- 2019-03-07
- 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
- 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 |
|---|
| 51655-266 | ALPRAZOLAM TABLET [NORTHWIND PHARMACEUTICALS] | 2 | Legacy NDC | 20220101_adc80020-091b-2419-e053-2a95a90adc6a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51655-266-52 | 51655026652 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-266-52) | 30 tablet | 2019-03-07 | 0000-00-00 | No | No | Current |