Lorazepam - 68788-9174-1 - (Lorazepam)

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Drug Information of Lorazepam

Product NDC: 68788-9174
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: 68788-9174
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072927
Marketing Category: ANDA
Start Marketing Date: 19911031

Package Information of Lorazepam

Package NDC: 68788-9174-1
Package Description: 15 TABLET in 1 BOTTLE, PLASTIC (68788-9174-1)

NDC Information of Lorazepam

NDC Code 68788-9174-1
Proprietary Name Lorazepam
Package Description 15 TABLET in 1 BOTTLE, PLASTIC (68788-9174-1)
Product NDC 68788-9174
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lorazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19911031
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name LORAZEPAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Lorazepam


General Information