"71335-0118-2" National Drug Code (NDC)

Labetalol Hydrochloride 60 TABLET in 1 BOTTLE (71335-0118-2)
(Bryant Ranch Prepack)

NDC Code71335-0118-2
Package Description60 TABLET in 1 BOTTLE (71335-0118-2)
Product NDC71335-0118
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20141201
Marketing Category NameNDA
Application NumberNDA018716
ManufacturerBryant Ranch Prepack
Substance NameLABETALOL HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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