Oxazepam - 0228-2073-10 - (Oxazepam)

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Drug Information of Oxazepam

Product NDC: 0228-2073
Proprietary Name: Oxazepam
Non Proprietary Name: Oxazepam
Active Ingredient(s): 30    mg/1 & nbsp;   Oxazepam
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Oxazepam

Product NDC: 0228-2073
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072253
Marketing Category: ANDA
Start Marketing Date: 20070102

Package Information of Oxazepam

Package NDC: 0228-2073-10
Package Description: 100 CAPSULE, GELATIN COATED in 1 BOTTLE (0228-2073-10)

NDC Information of Oxazepam

NDC Code 0228-2073-10
Proprietary Name Oxazepam
Package Description 100 CAPSULE, GELATIN COATED in 1 BOTTLE (0228-2073-10)
Product NDC 0228-2073
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxazepam
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20070102
Marketing Category Name ANDA
Labeler Name Actavis Elizabeth LLC
Substance Name OXAZEPAM
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Oxazepam


General Information