Triazolam - 63629-2956-2 - (Triazolam)

Alphabetical Index


Drug Information of Triazolam

Product NDC: 63629-2956
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: 63629-2956
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074224
Marketing Category: ANDA
Start Marketing Date: 19940601

Package Information of Triazolam

Package NDC: 63629-2956-2
Package Description: 30 TABLET in 1 BOTTLE (63629-2956-2)

NDC Information of Triazolam

NDC Code 63629-2956-2
Proprietary Name Triazolam
Package Description 30 TABLET in 1 BOTTLE (63629-2956-2)
Product NDC 63629-2956
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Triazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19940601
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name TRIAZOLAM
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Triazolam


General Information