PredniSONE - 76237-228-30 - (PredniSONE)

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Drug Information of PredniSONE

Product NDC: 76237-228
Proprietary Name: PredniSONE
Non Proprietary Name: PredniSONE
Active Ingredient(s): 10    mg/1 & nbsp;   PredniSONE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PredniSONE

Product NDC: 76237-228
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084122
Marketing Category: ANDA
Start Marketing Date: 20111220

Package Information of PredniSONE

Package NDC: 76237-228-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-228-30) > 5 TABLET in 1 BLISTER PACK

NDC Information of PredniSONE

NDC Code 76237-228-30
Proprietary Name PredniSONE
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-228-30) > 5 TABLET in 1 BLISTER PACK
Product NDC 76237-228
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PredniSONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111220
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name PREDNISONE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of PredniSONE


General Information