"51655-967-52" National Drug Code (NDC)

Alfuzosin Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-967-52)
(Northwind Pharmaceuticals, LLC)

NDC Code51655-967-52
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-967-52)
Product NDC51655-967
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlfuzosin Hydrochloride
Non-Proprietary NameAlfuzosin Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20230629
Marketing Category NameANDA
Application NumberANDA203192
ManufacturerNorthwind Pharmaceuticals, LLC
Substance NameALFUZOSIN HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesAdrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]

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