"53808-0733-1" National Drug Code (NDC)

Minoxidil 30 TABLET in 1 BLISTER PACK (53808-0733-1)
(DOH CENTRAL PHARMACY)

NDC Code53808-0733-1
Package Description30 TABLET in 1 BLISTER PACK (53808-0733-1)
Product NDC53808-0733
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMinoxidil
Non-Proprietary NameMinoxidil
Dosage FormTABLET
UsageORAL
Start Marketing Date20090701
Marketing Category NameANDA
Application NumberANDA071839
ManufacturerDOH CENTRAL PHARMACY
Substance NameMINOXIDIL
Strength10
Strength Unitmg/1
Pharmacy ClassesArteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

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