"67296-2114-6" National Drug Code (NDC)

Labetalol Hydrochloride 60 TABLET, FILM COATED in 1 BOTTLE (67296-2114-6)
(RedPharm Drug)

NDC Code67296-2114-6
Package Description60 TABLET, FILM COATED in 1 BOTTLE (67296-2114-6)
Product NDC67296-2114
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
ManufacturerRedPharm Drug
Substance NameLABETALOL HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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