"16571-856-90" National Drug Code (NDC)

Pentoxifylline 1 BLISTER PACK in 1 CARTON (16571-856-90) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(Rising Pharma Holdings, Inc.)

NDC Code16571-856-90
Package Description1 BLISTER PACK in 1 CARTON (16571-856-90) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC16571-856
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePentoxifylline
Non-Proprietary NamePentoxifylline
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20240611
Marketing Category NameANDA
Application NumberANDA074425
ManufacturerRising Pharma Holdings, Inc.
Substance NamePENTOXIFYLLINE
Strength400
Strength Unitmg/1
Pharmacy ClassesBlood Viscosity Reducer [EPC], Hematologic Activity Alteration [PE]

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