"70934-306-30" National Drug Code (NDC)

Alfuzosin Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-306-30)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-306-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-306-30)
Product NDC70934-306
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlfuzosin Hydrochloride
Non-Proprietary NameAlfuzosin Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20190321
Marketing Category NameANDA
Application NumberANDA079057
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameALFUZOSIN HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesAdrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]

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