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"61919-349-30" National Drug Code (NDC)

Alfuzosin Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-349-30)
(DirectRX)

NDC Code61919-349-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-349-30)
Product NDC61919-349
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlfuzosin Hydrochloride
Non-Proprietary NameAlfuzosin Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20151221
Marketing Category NameANDA
Application NumberANDA079057
ManufacturerDirectRX
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/61919-349-30





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