"72888-122-05" National Drug Code (NDC)

Labetalol Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (72888-122-05)
(Advagen Pharma Ltd)

NDC Code72888-122-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (72888-122-05)
Product NDC72888-122
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210818
Marketing Category NameANDA
Application NumberANDA211953
ManufacturerAdvagen Pharma Ltd
Substance NameLABETALOL HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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