Lorazepam - 0781-5408-05 - (Lorazepam)

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Drug Information of Lorazepam

Product NDC: 0781-5408
Proprietary Name: Lorazepam
Non Proprietary Name: Lorazepam
Active Ingredient(s): 2    mg/1 & nbsp;   Lorazepam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lorazepam

Product NDC: 0781-5408
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071141
Marketing Category: ANDA
Start Marketing Date: 20070108

Package Information of Lorazepam

Package NDC: 0781-5408-05
Package Description: 500 TABLET in 1 BOTTLE (0781-5408-05)

NDC Information of Lorazepam

NDC Code 0781-5408-05
Proprietary Name Lorazepam
Package Description 500 TABLET in 1 BOTTLE (0781-5408-05)
Product NDC 0781-5408
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lorazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070108
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name LORAZEPAM
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Lorazepam


General Information