Triazolam - 21695-303-10 - (Triazolam)

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Drug Information of Triazolam

Product NDC: 21695-303
Proprietary Name: Triazolam
Non Proprietary Name: Triazolam
Active Ingredient(s): .125    mg/1 & nbsp;   Triazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Triazolam

Product NDC: 21695-303
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074224
Marketing Category: ANDA
Start Marketing Date: 20090713

Package Information of Triazolam

Package NDC: 21695-303-10
Package Description: 10 TABLET in 1 BOTTLE (21695-303-10)

NDC Information of Triazolam

NDC Code 21695-303-10
Proprietary Name Triazolam
Package Description 10 TABLET in 1 BOTTLE (21695-303-10)
Product NDC 21695-303
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Triazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090713
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name TRIAZOLAM
Strength Number .125
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Triazolam


General Information