"55154-2339-0" National Drug Code (NDC)

Labetalol Hydrochloride 10 BLISTER PACK in 1 BAG (55154-2339-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
(Cardinal Health 107, LLC)

NDC Code55154-2339-0
Package Description10 BLISTER PACK in 1 BAG (55154-2339-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC55154-2339
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171205
Marketing Category NameANDA
Application NumberANDA207743
ManufacturerCardinal Health 107, LLC
Substance NameLABETALOL HYDROCHLORIDE
Strength200
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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