"71209-083-05" National Drug Code (NDC)

Labetalol Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (71209-083-05)
(Cadila Pharmaceuticals Limited)

NDC Code71209-083-05
Package Description100 TABLET, FILM COATED in 1 BOTTLE (71209-083-05)
Product NDC71209-083
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180529
Marketing Category NameANDA
Application NumberANDA211325
ManufacturerCadila Pharmaceuticals Limited
Substance NameLABETALOL HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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