Product NDC: | 54569-3966 |
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) |
Product NDC: | 54569-3966 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017892 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 19821115 |
Package NDC: | 54569-3966-3 |
Package Description: | 6 TABLET in 1 BOTTLE (54569-3966-3) |
NDC Code | 54569-3966-3 |
Proprietary Name | Triazolam |
Package Description | 6 TABLET in 1 BOTTLE (54569-3966-3) |
Product NDC | 54569-3966 |
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 | A-S Medication Solutions LLC |
Substance Name | TRIAZOLAM |
Strength Number | .25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |