Lorazepam - 49999-122-90 - (Lorazepam)

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Drug Information of Lorazepam

Product NDC: 49999-122
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: 49999-122
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072927
Marketing Category: ANDA
Start Marketing Date: 20110131

Package Information of Lorazepam

Package NDC: 49999-122-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (49999-122-90)

NDC Information of Lorazepam

NDC Code 49999-122-90
Proprietary Name Lorazepam
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (49999-122-90)
Product NDC 49999-122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lorazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110131
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name LORAZEPAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Lorazepam


General Information