Triazolam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Unit Dose Services. The primary component is Triazolam.
| Product ID | 50436-3718_f5b30aac-692e-4302-be23-c4987468182c |
| NDC | 50436-3718 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Triazolam |
| Generic Name | Triazolam |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 1982-11-15 |
| Marketing Category | NDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC |
| Application Number | NDA017892 |
| Labeler Name | Unit Dose Services |
| Substance Name | TRIAZOLAM |
| Active Ingredient Strength | 0 mg/1 |
| Pharm Classes | Benzodiazepine [EPC],Benzodiazepines [CS] |
| DEA Schedule | CIV |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2017-06-30 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA017892 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2017-06-30 |
| Ingredient | Strength |
|---|---|
| TRIAZOLAM | .25 mg/1 |
| SPL SET ID: | ce6ddb53-89ca-4edf-a519-553d34ce7938 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0054-4858 | Triazolam | Triazolam |
| 0054-4859 | Triazolam | Triazolam |
| 21695-284 | Triazolam | Triazolam |
| 21695-303 | Triazolam | Triazolam |
| 43063-996 | Triazolam | Triazolam |
| 43353-451 | Triazolam | triazolam |
| 50090-0522 | Triazolam | triazolam |
| 50090-4733 | Triazolam | Triazolam |
| 50436-3718 | Triazolam | triazolam |
| 50742-645 | Triazolam | Triazolam |
| 50742-646 | Triazolam | Triazolam |
| 55289-787 | Triazolam | triazolam |
| 59762-3717 | Triazolam | triazolam |
| 59762-3718 | Triazolam | triazolam |
| 67544-725 | Triazolam | Triazolam |
| 63629-2956 | Triazolam | Triazolam |
| 0009-0017 | Halcion | triazolam |