Alprazolam
- Product NDC
- 0904-5859
- 11-digit product format
- 009045859
- Labeler code
- 0904
- Product ID
- 0904-5859_e2a94e71-76f4-4129-a73f-14931500da1a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA074342
- Marketing category
- ANDA
- Marketing start
- 2008-04-02
- Marketing end
- 2021-05-31
- Substance
- ALPRAZOLAM
- Active strength
- 1 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 |
|---|
| 0904-5859-61 | 00904585961 | 100 BLISTER PACK in 1 CARTON (0904-5859-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2008-04-02 | 2021-05-31 | No | No | Current |