Lorazepam - 21695-239-03 - (Lorazepam)

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Drug Information of Lorazepam

Product NDC: 21695-239
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: 21695-239
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071194
Marketing Category: ANDA
Start Marketing Date: 19880415

Package Information of Lorazepam

Package NDC: 21695-239-03
Package Description: 3 TABLET in 1 BOTTLE (21695-239-03)

NDC Information of Lorazepam

NDC Code 21695-239-03
Proprietary Name Lorazepam
Package Description 3 TABLET in 1 BOTTLE (21695-239-03)
Product NDC 21695-239
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lorazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880415
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name LORAZEPAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Lorazepam


General Information