Triazolam - 59762-3718-4 - (triazolam)

Alphabetical Index


Drug Information of Triazolam

Product NDC: 59762-3718
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: 59762-3718
Labeler Name: Greenstone 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: 59762-3718-4
Package Description: 10 BOTTLE in 1 PACKAGE (59762-3718-4) > 10 TABLET in 1 BOTTLE

NDC Information of Triazolam

NDC Code 59762-3718-4
Proprietary Name Triazolam
Package Description 10 BOTTLE in 1 PACKAGE (59762-3718-4) > 10 TABLET in 1 BOTTLE
Product NDC 59762-3718
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 Greenstone LLC
Substance Name TRIAZOLAM
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Triazolam


General Information