Triazolam
- Product NDC
- 72789-349
- 11-digit product format
- 727890349
- Labeler code
- 72789
- Product ID
- 72789-349_40bb635a-95e9-a7d3-e063-6294a90a6ed5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- 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 |
|---|
| 72789-349-30 | 72789034930 | 30 TABLET in 1 BOTTLE, PLASTIC (72789-349-30) | 30 tablet | 2023-08-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Triazolam | PD-Rx Pharmaceuticals, Inc. | 2025-10-09 | HUMAN PRESCRIPTION DRUG LABEL | 10 |
| Triazolam | PD-Rx Pharmaceuticals, Inc. | 2024-10-09 | HUMAN PRESCRIPTION DRUG LABEL | 9 |