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"47335-956-88" National Drug Code (NDC)

Alfuzosin Hydrochloride 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-88)
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-956-88
Package Description100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-88)
Product NDC47335-956
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlfuzosin Hydrochloride
Non-Proprietary NameAlfuzosin Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20111122
Marketing Category NameANDA
Application NumberANDA079057
ManufacturerSun Pharmaceutical Industries, 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/47335-956-88





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