"70377-060-13" National Drug Code (NDC)

Labetalol Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (70377-060-13)
(Biocon Pharma Inc.)

NDC Code70377-060-13
Package Description500 TABLET, FILM COATED in 1 BOTTLE (70377-060-13)
Product NDC70377-060
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210527
Marketing Category NameANDA
Application NumberANDA209603
ManufacturerBiocon Pharma Inc.
Substance NameLABETALOL HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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