Alprazolam
- Product NDC
- 55700-929
- 11-digit product format
- 557000929
- Labeler code
- 55700
- Product ID
- 55700-929_3daaca7c-cd25-4037-b74e-8e00eba3ed52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA074342
- Marketing category
- ANDA
- Marketing start
- 2021-09-09
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55700-929 | ALPRAZOLAM TABLET [QUALITY CARE PRODUCTS, LLC] | 4 | Legacy NDC | 20241220_82f848c2-d3aa-4572-85b3-9f897515fc2e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-929-30 | 55700092930 | 30 TABLET in 1 BOTTLE (55700-929-30) | 30 tablet | 2021-09-09 | 0000-00-00 | No | No | Current |