Triazolam
- Product NDC
- 50090-7787
- 11-digit product format
- 500907787
- Labeler code
- 50090
- Product ID
- 50090-7787_06d8619e-5eaf-482f-b7bc-d2b44c8be8ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
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 |
|---|
| 50090-7787-0 | Triazolam | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 50090-7787-1 | Triazolam | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7787-0 | 50090778700 | 30 TABLET in 1 BOTTLE (50090-7787-0) | 30 tablet | 2025-11-24 | No | No | Historical |
| 50090-7787-1 | 50090778701 | 100 TABLET in 1 BOTTLE (50090-7787-1) | 100 tablet | 2025-11-24 | No | No | Historical |