Lorazepam - 0603-4247-32 - (Lorazepam)

Alphabetical Index


Drug Information of Lorazepam

Product NDC: 0603-4247
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: 0603-4247
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077754
Marketing Category: ANDA
Start Marketing Date: 20060510

Package Information of Lorazepam

Package NDC: 0603-4247-32
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (0603-4247-32)

NDC Information of Lorazepam

NDC Code 0603-4247-32
Proprietary Name Lorazepam
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (0603-4247-32)
Product NDC 0603-4247
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lorazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060510
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name LORAZEPAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Lorazepam


General Information