Triazolam - 54569-3966-0 - (triazolam)

Alphabetical Index


Drug Information of Triazolam

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)

Labeler Information of Triazolam

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 Information of Triazolam

Package NDC: 54569-3966-0
Package Description: 30 TABLET in 1 BOTTLE (54569-3966-0)

NDC Information of Triazolam

NDC Code 54569-3966-0
Proprietary Name Triazolam
Package Description 30 TABLET in 1 BOTTLE (54569-3966-0)
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]

Complete Information of Triazolam


General Information