Alprazolam
- Product NDC
- 17856-2029
- 11-digit product format
- 178562029
- Labeler code
- 17856
- Product ID
- 17856-2029_5f6b83ec-c858-46d6-9084-41d54701de47
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- ANDA074342
- Marketing category
- ANDA
- Marketing start
- 1993-10-01
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17856-2029-1 | Alprazolam | 100 in 1 BOX, UNIT-DOSE | TABLET | 100 | | 2 |
| 17856-2029-1 | Alprazolam | 1 in 1 POUCH | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-2029 | ALPRAZOLAM TABLET [ATLANTIC BIOLOGICALS CORP.] | 2 | Legacy NDC, 2 package rows | 20240515_3c367c14-bcc3-4c02-baa1-d6a0f3998697.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17856-2029-1 | 17856202901 | 100 POUCH in 1 BOX, UNIT-DOSE (17856-2029-1) > 1 TABLET in 1 POUCH | 100 pouch | 2020-08-25 | 0000-00-00 | No | No | Current |