Triazolam
- Product NDC
- 50090-6471
- 11-digit product format
- 500906471
- Labeler code
- 50090
- Product ID
- 50090-6471_c9dae524-0feb-4ff7-beba-8d28fde03cae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA214219
- Marketing category
- ANDA
- Marketing start
- 2020-10-20
- Substance
- TRIAZOLAM
- Active strength
- .25 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 1HM943223R | TRIAZOLAM | 28911-01-5 | TRIAZOLAM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6471-0 | 50090647100 | 30 TABLET in 1 BOTTLE (50090-6471-0) | 30 tablet | 2023-05-09 | No | No | Historical |
| 50090-6471-1 | 50090647101 | 100 TABLET in 1 BOTTLE (50090-6471-1) | 100 tablet | 2023-05-09 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Triazolam | A-S Medication Solutions | 2023-05-11 | HUMAN PRESCRIPTION DRUG LABEL | 1 |