Alprazolam
- Product NDC
- 70518-2870
- 11-digit product format
- 705182870
- Labeler code
- 70518
- Product ID
- 70518-2870_d782069e-d3c7-593b-e053-2a95a90a1473
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090871
- Marketing category
- ANDA
- Marketing start
- 2020-09-08
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2870-0 | 70518287000 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2870-0) | 2020-09-08 | 0000-00-00 | No | No | Current |