Alprazolam
- Product NDC
- 70518-0966
- 11-digit product format
- 705180966
- Labeler code
- 70518
- Product ID
- 70518-0966_a5b53ed9-1258-0ede-e053-2995a90a2c52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074174
- Marketing category
- ANDA
- Marketing start
- 2018-01-18
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 70518-0966-0 | 70518096600 | 30 TABLET in 1 BLISTER PACK (70518-0966-0) | 30 tablet | 2018-01-18 | 0000-00-00 | No | No | Current |