Alprazolam
- Product NDC
- 72789-087
- 11-digit product format
- 727890087
- Labeler code
- 72789
- Product ID
- 72789-087_e57fed22-eb43-7417-e053-2a95a90adf23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA018276
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1981-10-16
- 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
- 2023-12-31
- 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 |
|---|
| 72789-087-06 | 72789008706 | 6 TABLET in 1 BOTTLE, PLASTIC (72789-087-06) | 6 tablet | 2020-07-14 | 0000-00-00 | No | No | Current |
| 72789-087-30 | 72789008730 | 30 TABLET in 1 BOTTLE, PLASTIC (72789-087-30) | 30 tablet | 2020-06-05 | 0000-00-00 | No | No | Current |