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Pentoxifylline - 55154-5483-0 - (Pentoxifylline)

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Drug Information of Pentoxifylline

Product NDC: 55154-5483
Proprietary Name: Pentoxifylline
Non Proprietary Name: Pentoxifylline
Active Ingredient(s): 400    mg/1 & nbsp;   Pentoxifylline
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Pentoxifylline

Product NDC: 55154-5483
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074425
Marketing Category: ANDA
Start Marketing Date: 20100723

Package Information of Pentoxifylline

Package NDC: 55154-5483-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5483-0) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Pentoxifylline

NDC Code 55154-5483-0
Proprietary Name Pentoxifylline
Package Description 10 BLISTER PACK in 1 BAG (55154-5483-0) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 55154-5483
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pentoxifylline
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100723
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name PENTOXIFYLLINE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE]

Complete Information of Pentoxifylline


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