Alprazolam
- Product NDC
- 55154-5885
- 11-digit product format
- 551545885
- Labeler code
- 55154
- Product ID
- 55154-5885_a386ebf8-a752-4107-ab5d-230fe6387b1a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA074342
- Marketing category
- ANDA
- Marketing start
- 2008-04-02
- 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
- 2021-12-31
- 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 |
|---|
| 55154-5885-0 | 55154588500 | 10 BLISTER PACK in 1 BAG (55154-5885-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2008-04-02 | 0000-00-00 | No | No | Current |