Alprazolam
- Product NDC
- 67253-902
- 11-digit product format
- 672530902
- Labeler code
- 67253
- Product ID
- 67253-902_f7f35ad6-705d-4e9e-9ace-6c5eedf6459e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Par Pharmaceutical
- Application
- ANDA074174
- Marketing category
- ANDA
- Marketing start
- 2007-03-28
- Marketing end
- 2022-06-30
- 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
DailyMed Product Concepts#
DailyMed Socrata Ingredients#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67253-902-10 | 67253090210 | 100 TABLET in 1 BOTTLE (67253-902-10) | 100 tablet | 2007-03-28 | 2022-05-31 | No | No | Current |
| 67253-902-11 | 67253090211 | 1000 TABLET in 1 BOTTLE (67253-902-11) | 1000 tablet | 2007-03-28 | 2022-06-30 | No | No | Current |
| 67253-902-50 | 67253090250 | 500 TABLET in 1 BOTTLE (67253-902-50) | 500 tablet | 2007-03-28 | 2022-04-30 | No | No | Current |