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"63629-2354-1" National Drug Code (NDC)

Alfuzosin Hydrochloride 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2354-1)
(Bryant Ranch Prepack)

NDC Code63629-2354-1
Package Description100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2354-1)
Product NDC63629-2354
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlfuzosin Hydrochloride
Non-Proprietary NameAlfuzosin Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20111122
End Marketing Date20240831
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/63629-2354-1





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