Alprazolam
- Product NDC
- 0615-8216
- 11-digit product format
- 006158216
- Labeler code
- 0615
- Product ID
- 0615-8216_0cd8cee6-159e-4bd3-9f6e-fa15fc0aea33
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA203346
- Marketing category
- ANDA
- Marketing start
- 2018-06-05
- Marketing end
- 2023-06-30
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8216-39 | 00615821639 | 30 TABLET in 1 BLISTER PACK (0615-8216-39) | 30 tablet | 2018-06-05 | 2023-06-30 | No | No | Current |