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"52125-170-02" National Drug Code (NDC)

Minoxidil 30 TABLET in 1 BLISTER PACK (52125-170-02)
(REMEDYREPACK INC.)

NDC Code52125-170-02
Package Description30 TABLET in 1 BLISTER PACK (52125-170-02)
Product NDC52125-170
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMinoxidil
Non-Proprietary NameMinoxidil
Dosage FormTABLET
UsageORAL
Start Marketing Date20130320
Marketing Category NameANDA
Application NumberANDA072709
ManufacturerREMEDYREPACK INC.
Substance NameMINOXIDIL
Strength10
Strength Unitmg/1
Pharmacy ClassesArteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-170-02





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