Lorazepam - 51079-387-20 - (lorazepam)

Alphabetical Index


Drug Information of Lorazepam

Product NDC: 51079-387
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: 51079-387
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077657
Marketing Category: ANDA
Start Marketing Date: 20101217

Package Information of Lorazepam

Package NDC: 51079-387-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-387-20) > 1 TABLET in 1 BLISTER PACK (51079-387-01)

NDC Information of Lorazepam

NDC Code 51079-387-20
Proprietary Name Lorazepam
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-387-20) > 1 TABLET in 1 BLISTER PACK (51079-387-01)
Product NDC 51079-387
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lorazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101217
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name LORAZEPAM
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Lorazepam


General Information