Triazolam
- Product NDC
- 50436-3718
- 11-digit product format
- 504363718
- Labeler code
- 50436
- Product ID
- 50436-3718_f5b30aac-692e-4302-be23-c4987468182c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- triazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- NDA017892
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1982-11-15
- Marketing end
- 0000-00-00
- Substance
- TRIAZOLAM
- Active strength
- 0 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-3718-1 | Triazolam | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-3718 | TRIAZOLAM TABLET [UNIT DOSE SERVICES] | 4 | Legacy NDC, 1 package rows | 20171109_ce6ddb53-89ca-4edf-a519-553d34ce7938.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-3718-1 | 50436371801 | 30 in 1 BOTTLE | Historical |