NDC 51079-889

Pentoxifylline

Pentoxifylline

Pentoxifylline is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Mylan Institutional Inc.. The primary component is Pentoxifylline.

Product ID51079-889_7d7c9caf-523a-f8c3-e053-2a91aa0a7aa1
NDC51079-889
Product TypeHuman Prescription Drug
Proprietary NamePentoxifylline
Generic NamePentoxifylline
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date1998-01-15
Marketing End Date2019-05-31
Marketing CategoryANDA / ANDA
Application NumberANDA074425
Labeler NameMylan Institutional Inc.
Substance NamePENTOXIFYLLINE
Active Ingredient Strength400 mg/1
Pharm ClassesBlood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE]
NDC Exclude FlagN

Packaging

NDC 51079-889-20

100 BLISTER PACK in 1 CARTON (51079-889-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-889-01)
Marketing Start Date1998-01-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51079-889-20 [51079088920]

Pentoxifylline TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074425
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-01-15
Marketing End Date2019-05-31

NDC 51079-889-01 [51079088901]

Pentoxifylline TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074425
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-01-15
Marketing End Date2019-05-31

NDC 51079-889-19 [51079088919]

Pentoxifylline TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074425
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-01-15
Marketing End Date2017-05-31

NDC 51079-889-17 [51079088917]

Pentoxifylline TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074425
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-01-15
Marketing End Date2018-12-20

Drug Details

Active Ingredients

IngredientStrength
PENTOXIFYLLINE400 mg/1

OpenFDA Data

SPL SET ID:81a0e173-0dc6-4d46-a699-37d2ac5b4df1
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 312301
  • Pharmacological Class

    • Blood Viscosity Reducer [EPC]
    • Hematologic Activity Alteration [PE]

    Medicade Reported Pricing

    51079088920 PENTOXIFYLLINE ER 400 MG TAB

    Pricing Unit: EA | Drug Type:

    51079088919 PENTOXIFYLLINE ER 400 MG TAB

    Pricing Unit: EA | Drug Type:

    51079088917 PENTOXIFYLLINE ER 400 MG TAB

    Pricing Unit: EA | Drug Type:

    51079088901 PENTOXIFYLLINE ER 400 MG TAB

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Pentoxifylline" or generic name "Pentoxifylline"

    NDCBrand NameGeneric Name
    0378-0357PentoxifyllinePentoxifylline
    0615-4523PentoxifyllinePentoxifylline
    0615-8305PENTOXIFYLLINEPENTOXIFYLLINE
    0904-5448PENTOXIFYLLINEPENTOXIFYLLINE
    33261-992PENTOXIFYLLINEPENTOXIFYLLINE
    43353-123PentoxifyllinePentoxifylline
    51079-889PentoxifyllinePentoxifylline
    53808-0516PentoxifyllinePentoxifylline
    53808-0757PentoxifyllinePENTOXIFYLLINE
    53808-0758PentoxifyllinePentoxifylline
    60429-703PENTOXIFYLLINEPENTOXIFYLLINE
    60505-0033PENTOXIFYLLINEPENTOXIFYLLINE
    63629-2910PENTOXIFYLLINEPENTOXIFYLLINE
    66267-710PENTOXIFYLLINEPENTOXIFYLLINE
    67544-252PENTOXIFYLLINEPENTOXIFYLLINE
    68071-4532PentoxifyllinePentoxifylline
    68682-101PentoxifyllinePentoxifylline
    68788-9742PENTOXIFYLLINEPENTOXIFYLLINE
    70518-1285PENTOXIFYLLINEPENTOXIFYLLINE
    72189-025PENTOXIFYLLINEPENTOXIFYLLINE

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