"42806-329-10" National Drug Code (NDC)

Labetalol Hydrochloride 1000 TABLET in 1 BOTTLE (42806-329-10)
(Epic Pharma, LLC)

NDC Code42806-329-10
Package Description1000 TABLET in 1 BOTTLE (42806-329-10)
Product NDC42806-329
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20210930
Marketing Category NameANDA
Application NumberANDA212990
ManufacturerEpic Pharma, LLC
Substance NameLABETALOL HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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