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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Triazolam
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TRIAZOLAM | .25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1HM943223R |
| Rxcui | 198318 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-349-30 | Triazolam | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-349 | TRIAZOLAM TABLET [PD-RX PHARMACEUTICALS, INC.] | 9 | Current NDC, 1 package rows | 20241011_f8ca4773-e201-4cb9-8869-5ee07ba1d0bf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |