Triazolam
- Product NDC
- 82804-275
- 11-digit product format
- 828040275
- Labeler code
- 82804
- Product ID
- 82804-275_ba1d8955-41f8-4b4d-8ed8-e92667e294a1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Triazolam
- Listing expiration
- 2027-12-31
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 |
|---|
| 82804-275-30 | Triazolam | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 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 |
|---|
| 82804-275-30 | 82804027530 | 30 TABLET in 1 BOTTLE, PLASTIC (82804-275-30) | 30 tablet | 2020-10-20 | No | No | Historical |