Oxazepam - 0781-2809-10 - (Oxazepam)

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Drug Information of Oxazepam

Product NDC: 0781-2809
Proprietary Name: Oxazepam
Non Proprietary Name: Oxazepam
Active Ingredient(s): 10    mg/1 & nbsp;   Oxazepam
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Oxazepam

Product NDC: 0781-2809
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071813
Marketing Category: ANDA
Start Marketing Date: 19880419

Package Information of Oxazepam

Package NDC: 0781-2809-10
Package Description: 1000 CAPSULE in 1 BOTTLE (0781-2809-10)

NDC Information of Oxazepam

NDC Code 0781-2809-10
Proprietary Name Oxazepam
Package Description 1000 CAPSULE in 1 BOTTLE (0781-2809-10)
Product NDC 0781-2809
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxazepam
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19880419
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name OXAZEPAM
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Oxazepam


General Information