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"42291-619-10" National Drug Code (NDC)

Minoxidil 1000 TABLET in 1 BOTTLE (42291-619-10)
(AvKARE, Inc.)

NDC Code42291-619-10
Package Description1000 TABLET in 1 BOTTLE (42291-619-10)
Product NDC42291-619
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMinoxidil
Non-Proprietary NameMinoxidil
Dosage FormTABLET
UsageORAL
Start Marketing Date20130801
Marketing Category NameANDA
Application NumberANDA072709
ManufacturerAvKARE, 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/42291-619-10





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