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oxandrolone - 0245-0272-01 - (oxandrolone)

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Drug Information of oxandrolone

Product NDC: 0245-0272
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: 0245-0272
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078033
Marketing Category: ANDA
Start Marketing Date: 20070322

Package Information of oxandrolone

Package NDC: 0245-0272-01
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0245-0272-01) > 10 TABLET in 1 BLISTER PACK (0245-0272-89)

NDC Information of oxandrolone

NDC Code 0245-0272-01
Proprietary Name oxandrolone
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0245-0272-01) > 10 TABLET in 1 BLISTER PACK (0245-0272-89)
Product NDC 0245-0272
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxandrolone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070322
Marketing Category Name ANDA
Labeler Name Upsher-Smith Laboratories, Inc.
Substance Name OXANDROLONE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of oxandrolone


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