Xanax
- Product NDC
- 0009-0068
- 11-digit product format
- 000090068
- Labeler code
- 0009
- Product ID
- 0009-0068_f364e489-b47b-4283-a7fe-d5b15f77447e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- alprazolam
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Pharmacia & Upjohn Company LLC
- Application
- NDA021434
- Marketing category
- NDA
- Marketing start
- 2003-01-17
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 3 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0009-0068-07 | 00009006807 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0009-0068-07) | 2003-01-17 | 0000-00-00 | No | No | Current |