Triazolam - 49999-055-02 - (Triazolam)

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Drug Information of Triazolam

Product NDC: 49999-055
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: 49999-055
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074224
Marketing Category: ANDA
Start Marketing Date: 20110601

Package Information of Triazolam

Package NDC: 49999-055-02
Package Description: 2 TABLET in 1 BOTTLE, PLASTIC (49999-055-02)

NDC Information of Triazolam

NDC Code 49999-055-02
Proprietary Name Triazolam
Package Description 2 TABLET in 1 BOTTLE, PLASTIC (49999-055-02)
Product NDC 49999-055
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Triazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110601
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name TRIAZOLAM
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Triazolam


General Information