Lorazepam - 76237-289-39 - (lorazepam)

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Drug Information of Lorazepam

Product NDC: 76237-289
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: 76237-289
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077657
Marketing Category: ANDA
Start Marketing Date: 20120828

Package Information of Lorazepam

Package NDC: 76237-289-39
Package Description: 30 TABLET in 1 BLISTER PACK (76237-289-39)

NDC Information of Lorazepam

NDC Code 76237-289-39
Proprietary Name Lorazepam
Package Description 30 TABLET in 1 BLISTER PACK (76237-289-39)
Product NDC 76237-289
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lorazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120828
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name LORAZEPAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Lorazepam


General Information