Lorazepam - 63739-804-41 - (Lorazepam)

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Drug Information of Lorazepam

Product NDC: 63739-804
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: 63739-804
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078203
Marketing Category: ANDA
Start Marketing Date: 20110701

Package Information of Lorazepam

Package NDC: 63739-804-41
Package Description: 30 TABLET in 1 BOTTLE (63739-804-41)

NDC Information of Lorazepam

NDC Code 63739-804-41
Proprietary Name Lorazepam
Package Description 30 TABLET in 1 BOTTLE (63739-804-41)
Product NDC 63739-804
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lorazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110701
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
Substance Name LORAZEPAM
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Lorazepam


General Information