Triazolam
- Product NDC
- 70710-1289
- 11-digit product format
- 707101289
- Labeler code
- 70710
- Product ID
- 70710-1289_4c2fb12f-623b-4dc9-a9e0-7fac953f5cf0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA213003
- Marketing category
- ANDA
- Marketing start
- 2022-12-30
- 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 |
|---|
| 70710-1289-1 | 70710128901 | 100 TABLET in 1 BOTTLE (70710-1289-1) | 100 tablet | 2022-12-30 | No | No | Historical |
| 70710-1289-5 | 70710128905 | 500 TABLET in 1 BOTTLE (70710-1289-5) | 500 tablet | 2022-12-30 | No | No | Historical |
| 70710-1289-8 | 70710128908 | 10 TABLET in 1 BOTTLE (70710-1289-8) | 10 tablet | 2022-12-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Triazolam | A-S Medication Solutions | 2025-11-26 | HUMAN PRESCRIPTION DRUG LABEL | 1 |
| Triazolam | Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | 2023-02-10 | HUMAN PRESCRIPTION DRUG LABEL | 2 |