Triazolam - 54569-6376-0 - (Triazolam)

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Drug Information of Triazolam

Product NDC: 54569-6376
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: 54569-6376
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074224
Marketing Category: ANDA
Start Marketing Date: 19940601

Package Information of Triazolam

Package NDC: 54569-6376-0
Package Description: 20 TABLET in 1 BLISTER PACK (54569-6376-0)

NDC Information of Triazolam

NDC Code 54569-6376-0
Proprietary Name Triazolam
Package Description 20 TABLET in 1 BLISTER PACK (54569-6376-0)
Product NDC 54569-6376
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 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