"70771-1164-1" National Drug Code (NDC)

Labetalol Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (70771-1164-1)
(Zydus Lifesciences Limited)

NDC Code70771-1164-1
Package Description100 TABLET, FILM COATED in 1 BOTTLE (70771-1164-1)
Product NDC70771-1164
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171205
Marketing Category NameANDA
Application NumberANDA207743
ManufacturerZydus Lifesciences Limited
Substance NameLABETALOL HYDROCHLORIDE
Strength200
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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