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"51079-889-19" National Drug Code (NDC)

Pentoxifylline 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-889-19) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-889-17)
(Mylan Institutional Inc.)

NDC Code51079-889-19
Package Description25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-889-19) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-889-17)
Product NDC51079-889
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePentoxifylline
Non-Proprietary NamePentoxifylline
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date19980115
Marketing Category NameANDA
Application NumberANDA074425
ManufacturerMylan Institutional Inc.
Substance NamePENTOXIFYLLINE
Strength400
Strength Unitmg/1
Pharmacy ClassesBlood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE]

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