Home > National Drug Code (NDC) > Oxandrolone

Oxandrolone - 49884-302-02 - (oxandrolone)

Alphabetical Index


Drug Information of Oxandrolone

Product NDC: 49884-302
Proprietary Name: Oxandrolone
Non Proprietary Name: oxandrolone
Active Ingredient(s): 10    mg/1 & nbsp;   oxandrolone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Oxandrolone

Product NDC: 49884-302
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077827
Marketing Category: ANDA
Start Marketing Date: 20070820

Package Information of Oxandrolone

Package NDC: 49884-302-02
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (49884-302-02)

NDC Information of Oxandrolone

NDC Code 49884-302-02
Proprietary Name Oxandrolone
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (49884-302-02)
Product NDC 49884-302
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxandrolone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070820
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc.
Substance Name OXANDROLONE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Oxandrolone


General Information