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"53808-0733-1" National Drug Code (NDC)
Minoxidil 30 TABLET in 1 BLISTER PACK (53808-0733-1)
(DOH CENTRAL PHARMACY)
NDC Code
53808-0733-1
Package Description
30 TABLET in 1 BLISTER PACK (53808-0733-1)
Product NDC
53808-0733
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Minoxidil
Non-Proprietary Name
Minoxidil
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20090701
Marketing Category Name
ANDA
Application Number
ANDA071839
Manufacturer
DOH CENTRAL PHARMACY
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/53808-0733-1