Triazolam
- Product NDC
- 50090-4733
- 11-digit product format
- 500904733
- Labeler code
- 50090
- Product ID
- 50090-4733_2f2e5af4-5f57-44f2-92b9-b58170ec03cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074224
- Marketing category
- ANDA
- Marketing start
- 2018-10-29
- Marketing end
- 0000-00-00
- Substance
- TRIAZOLAM
- Active strength
- 0 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4733 | TRIAZOLAM TABLET [A-S MEDICATION SOLUTIONS] | 5 | Legacy NDC | 20230208_8828406e-89f0-458f-841f-4c041df4acda.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4733-0 | 50090473300 | 30 TABLET in 1 BOTTLE (50090-4733-0) | 30 tablet | 2019-11-18 | 0000-00-00 | No | No | Current |
| 50090-4733-1 | 50090473301 | 100 TABLET in 1 BOTTLE (50090-4733-1) | 100 tablet | 2019-11-18 | 0000-00-00 | No | No | Current |