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"71335-1529-4" National Drug Code (NDC)

Alfuzosin Hydrochloride 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1529-4)
(Bryant Ranch Prepack)

NDC Code71335-1529-4
Package Description120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1529-4)
Product NDC71335-1529
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/71335-1529-4





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