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Perrigo Prednisone - 10768-7085-1 - (Prednisone)

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Drug Information of Perrigo Prednisone

Product NDC: 10768-7085
Proprietary Name: Perrigo Prednisone
Non Proprietary Name: Prednisone
Active Ingredient(s): 20    mg/1 & nbsp;   Prednisone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Perrigo Prednisone

Product NDC: 10768-7085
Labeler Name: Perrigo Pharmaceuticals Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083677
Marketing Category: ANDA
Start Marketing Date: 20061011

Package Information of Perrigo Prednisone

Package NDC: 10768-7085-1
Package Description: 100 TABLET in 1 BOTTLE (10768-7085-1)

NDC Information of Perrigo Prednisone

NDC Code 10768-7085-1
Proprietary Name Perrigo Prednisone
Package Description 100 TABLET in 1 BOTTLE (10768-7085-1)
Product NDC 10768-7085
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20061011
Marketing Category Name ANDA
Labeler Name Perrigo Pharmaceuticals Company
Substance Name PREDNISONE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Perrigo Prednisone


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