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"51079-889-20" National Drug Code (NDC)
Pentoxifylline 100 BLISTER PACK in 1 CARTON (51079-889-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-889-01)
(Mylan Institutional Inc.)
NDC Code
51079-889-20
Package Description
100 BLISTER PACK in 1 CARTON (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
Proprietary Name
Pentoxifylline
Non-Proprietary Name
Pentoxifylline
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
19980115
End Marketing Date
20190531
Marketing Category Name
ANDA
Application Number
ANDA074425
Manufacturer
Mylan Institutional Inc.
Substance Name
PENTOXIFYLLINE
Strength
400
Strength Unit
mg/1
Pharmacy Classes
Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51079-889-20