Alprazolam
- Product NDC
- 70934-558
- 11-digit product format
- 709340558
- Labeler code
- 70934
- Product ID
- 70934-558_ee89ff26-f0de-cce6-e053-2a95a90a149a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA207507
- Marketing category
- ANDA
- Marketing start
- 2020-02-24
- Marketing end
- 2023-01-31
- Substance
- ALPRAZOLAM
- Active strength
- 0 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-558-30 | 70934055830 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-558-30) | 30 tablet | 2020-02-24 | 0000-00-00 | No | No | Current |