Tranxene - 67386-301-01 - (clorazepate dipotassium)

Alphabetical Index


Drug Information of Tranxene

Product NDC: 67386-301
Proprietary Name: Tranxene
Non Proprietary Name: clorazepate dipotassium
Active Ingredient(s): 3.75    mg/1 & nbsp;   clorazepate dipotassium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Tranxene

Product NDC: 67386-301
Labeler Name: Lundbeck Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017105
Marketing Category: NDA
Start Marketing Date: 19720623

Package Information of Tranxene

Package NDC: 67386-301-01
Package Description: 100 TABLET in 1 BOTTLE (67386-301-01)

NDC Information of Tranxene

NDC Code 67386-301-01
Proprietary Name Tranxene
Package Description 100 TABLET in 1 BOTTLE (67386-301-01)
Product NDC 67386-301
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clorazepate dipotassium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19720623
Marketing Category Name NDA
Labeler Name Lundbeck Inc.
Substance Name CLORAZEPATE DIPOTASSIUM
Strength Number 3.75
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Tranxene


General Information