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"52125-214-02" National Drug Code (NDC)
Pentoxifylline 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-214-02)
(REMEDYREPACK INC.)
NDC Code
52125-214-02
Package Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-214-02)
Product NDC
52125-214
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
20130329
Marketing Category Name
ANDA
Application Number
ANDA074425
Manufacturer
REMEDYREPACK 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/52125-214-02