"53489-386-03" National Drug Code (NDC)

Minoxidil 250 TABLET in 1 BOTTLE (53489-386-03)
(Sun Pharmaceutical Industries, Inc.)

NDC Code53489-386-03
Package Description250 TABLET in 1 BOTTLE (53489-386-03)
Product NDC53489-386
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMinoxidil
Non-Proprietary NameMinoxidil
Dosage FormTABLET
UsageORAL
Start Marketing Date19951214
Marketing Category NameANDA
Application NumberANDA072709
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameMINOXIDIL
Strength2.5
Strength Unitmg/1
Pharmacy ClassesArteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]

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