Home
>
National Drug Code (NDC)
>
TRIAZOLAM
TRIAZOLAM - 16590-236-60 - (TRIAZOLAM)
Drug Information of TRIAZOLAM
| Product NDC: | 16590-236 |
| Proprietary Name: | TRIAZOLAM |
| Non Proprietary Name: | TRIAZOLAM |
| Active Ingredient(s): | .25 mg/1 & nbsp; TRIAZOLAM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TRIAZOLAM
| Product NDC: | 16590-236 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017892 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19821115 |
Package Information of TRIAZOLAM
| Package NDC: | 16590-236-60 |
| Package Description: | 60 TABLET in 1 BOTTLE (16590-236-60) |
NDC Information of TRIAZOLAM
| NDC Code | 16590-236-60 |
| Proprietary Name | TRIAZOLAM |
| Package Description | 60 TABLET in 1 BOTTLE (16590-236-60) |
| Product NDC | 16590-236 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TRIAZOLAM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19821115 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | STAT RX USA LLC |
| Substance Name | TRIAZOLAM |
| Strength Number | .25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
