"70377-063-12" National Drug Code (NDC)

Labetalol Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (70377-063-12)
(Biocon Pharma Inc.)

NDC Code70377-063-12
Package Description100 TABLET, FILM COATED in 1 BOTTLE (70377-063-12)
Product NDC70377-063
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20241202
Marketing Category NameANDA
Application NumberANDA209603
ManufacturerBiocon Pharma Inc.
Substance NameLABETALOL HYDROCHLORIDE
Strength400
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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