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"71335-2146-3" National Drug Code (NDC)

Alfuzosin Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-3)
(Bryant Ranch Prepack)

NDC Code71335-2146-3
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-3)
Product NDC71335-2146
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlfuzosin Hydrochloride
Non-Proprietary NameAlfuzosin Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20111122
Marketing Category NameANDA
Application NumberANDA079057
ManufacturerBryant Ranch Prepack
Substance NameALFUZOSIN HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesAdrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-2146-3





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