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Pentoxifylline - 51079-889-20 - (Pentoxifylline)

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Drug Information of Pentoxifylline

Product NDC: 51079-889
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: 51079-889
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074425
Marketing Category: ANDA
Start Marketing Date: 20100723

Package Information of Pentoxifylline

Package NDC: 51079-889-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-889-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-889-01)

NDC Information of Pentoxifylline

NDC Code 51079-889-20
Proprietary Name Pentoxifylline
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-889-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-889-01)
Product NDC 51079-889
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 UDL Laboratories, Inc.
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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