Lorazepam - 0093-4820-01 - (Lorazepam)

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Drug Information of Lorazepam

Product NDC: 0093-4820
Proprietary Name: Lorazepam
Non Proprietary Name: Lorazepam
Active Ingredient(s): .5    mg/1 & nbsp;   Lorazepam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lorazepam

Product NDC: 0093-4820
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077396
Marketing Category: ANDA
Start Marketing Date: 20070201

Package Information of Lorazepam

Package NDC: 0093-4820-01
Package Description: 100 TABLET in 1 BOTTLE (0093-4820-01)

NDC Information of Lorazepam

NDC Code 0093-4820-01
Proprietary Name Lorazepam
Package Description 100 TABLET in 1 BOTTLE (0093-4820-01)
Product NDC 0093-4820
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lorazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070201
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name LORAZEPAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Lorazepam


General Information