Alprazolam
- Product NDC
- 82804-027
- 11-digit product format
- 828040027
- Labeler code
- 82804
- Product ID
- 82804-027_60c90b4b-174f-4fd2-b65f-fc166c16bdc1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- NDA018276
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1981-10-16
- Substance
- ALPRAZOLAM
- Active strength
- .25 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| YU55MQ3IZY | ALPRAZOLAM | 28981-97-7 | ALPRAZOLAM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-027-30 | 82804002730 | 30 TABLET in 1 BOTTLE (82804-027-30) | 30 tablet | 2023-10-23 | No | No | Historical |
| 82804-027-60 | 82804002760 | 60 TABLET in 1 BOTTLE (82804-027-60) | 60 tablet | 2023-10-23 | No | No | Historical |
| 82804-027-90 | 82804002790 | 90 TABLET in 1 BOTTLE (82804-027-90) | 90 tablet | 2023-10-23 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Alprazolam | Proficient Rx LP | 2023-10-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |