"33342-515-11" National Drug Code (NDC)

Labetalol Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (33342-515-11)
(Macleods Pharmaceuticals Limited)

NDC Code33342-515-11
Package Description100 TABLET, FILM COATED in 1 BOTTLE (33342-515-11)
Product NDC33342-515
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20250923
Marketing Category NameANDA
Application NumberANDA217949
ManufacturerMacleods Pharmaceuticals Limited
Substance NameLABETALOL HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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