Triazolam - 0054-4859-51 - (Triazolam)

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Drug Information of Triazolam

Product NDC: 0054-4859
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: 0054-4859
Labeler Name: Roxane Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074224
Marketing Category: ANDA
Start Marketing Date: 19940601

Package Information of Triazolam

Package NDC: 0054-4859-51
Package Description: 10 TABLET in 1 BOTTLE (0054-4859-51)

NDC Information of Triazolam

NDC Code 0054-4859-51
Proprietary Name Triazolam
Package Description 10 TABLET in 1 BOTTLE (0054-4859-51)
Product NDC 0054-4859
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 Roxane Laboratories, Inc.
Substance Name TRIAZOLAM
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Triazolam


General Information