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"42291-110-10" National Drug Code (NDC)

Alfuzosin Hydrochloride 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-110-10)
(AvKARE, Inc.)

NDC Code42291-110-10
Package Description1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-110-10)
Product NDC42291-110
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlfuzosin Hydrochloride
Proprietary Name SuffixEr
Non-Proprietary NameAlfuzosin Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20120313
End Marketing Date20190430
Marketing Category NameANDA
Application NumberANDA079013
ManufacturerAvKARE, Inc.
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/42291-110-10





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