Alprazolam
- Product NDC
- 60687-521
- 11-digit product format
- 606870521
- Labeler code
- 60687
- Product ID
- 60687-521_95fa8edb-9f28-01d6-e053-2a95a90ae879
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA207507
- Marketing category
- ANDA
- Marketing start
- 2019-10-21
- 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
- 2020-12-31
- 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 |
|---|
| 60687-521-01 | 60687052101 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-521-01) > 1 TABLET in 1 BLISTER PACK (60687-521-11) | 100 blister pack | 2019-10-21 | 0000-00-00 | No | No | Current |