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PENTOXIFYLLINE - 0904-5448-61 - (PENTOXIFYLLINE)

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Drug Information of PENTOXIFYLLINE

Product NDC: 0904-5448
Proprietary Name: PENTOXIFYLLINE
Non Proprietary Name: PENTOXIFYLLINE
Active Ingredient(s): 400    mg/1 & nbsp;   PENTOXIFYLLINE
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of PENTOXIFYLLINE

Product NDC: 0904-5448
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075191
Marketing Category: ANDA
Start Marketing Date: 20040216

Package Information of PENTOXIFYLLINE

Package NDC: 0904-5448-61
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0904-5448-61)

NDC Information of PENTOXIFYLLINE

NDC Code 0904-5448-61
Proprietary Name PENTOXIFYLLINE
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0904-5448-61)
Product NDC 0904-5448
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PENTOXIFYLLINE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20040216
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name PENTOXIFYLLINE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE]

Complete Information of PENTOXIFYLLINE


General Information