Lorazepam - 65084-442-18 - (Lorazepam)

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Drug Information of Lorazepam

Product NDC: 65084-442
Proprietary Name: Lorazepam
Non Proprietary Name: Lorazepam
Active Ingredient(s): 1    mg/1 & nbsp;   Lorazepam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lorazepam

Product NDC: 65084-442
Labeler Name: Rx Pak Division of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078203
Marketing Category: ANDA
Start Marketing Date: 20091009

Package Information of Lorazepam

Package NDC: 65084-442-18
Package Description: 90 TABLET in 1 BOTTLE (65084-442-18)

NDC Information of Lorazepam

NDC Code 65084-442-18
Proprietary Name Lorazepam
Package Description 90 TABLET in 1 BOTTLE (65084-442-18)
Product NDC 65084-442
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lorazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091009
Marketing Category Name ANDA
Labeler Name Rx Pak Division of McKesson Corporation
Substance Name LORAZEPAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Lorazepam


General Information