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"52125-039-02" National Drug Code (NDC)
Minoxidil 30 TABLET in 1 BLISTER PACK (52125-039-02)
(REMEDYREPACK INC.)
NDC Code
52125-039-02
Package Description
30 TABLET in 1 BLISTER PACK (52125-039-02)
Product NDC
52125-039
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Minoxidil
Non-Proprietary Name
Minoxidil
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20130226
Marketing Category Name
ANDA
Application Number
ANDA071839
Manufacturer
REMEDYREPACK INC.
Substance Name
MINOXIDIL
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-039-02