Triazolam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Greenstone Llc. The primary component is Triazolam.
Product ID | 59762-3717_1ce1c400-4bf3-43da-8b0a-0fe8c6b17431 |
NDC | 59762-3717 |
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 / NDA AUTHORIZED GENERIC |
Application Number | NDA017892 |
Labeler Name | Greenstone LLC |
Substance Name | TRIAZOLAM |
Active Ingredient Strength | 0 mg/1 |
Pharm Classes | Benzodiazepine |
DEA Schedule | CIV |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2017-01-13 |
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 | 2017-01-13 |
Marketing Category | NDA AUTHORIZED GENERIC |
Application Number | NDA017892 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1982-11-15 |
Ingredient | Strength |
---|---|
TRIAZOLAM | .125 mg/1 |
SPL SET ID: | 5add318e-11b9-42f8-b052-0d8cebb32fcf |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
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 |