"63739-366-10" National Drug Code (NDC)

Labetalol Hcl 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-366-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(McKesson Corporation dba SKY Packaging)

NDC Code63739-366-10
Package Description10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-366-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC63739-366
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hcl
Non-Proprietary NameLabetalol Hcl
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19980804
End Marketing Date20210630
Marketing Category NameANDA
Application NumberANDA075113
ManufacturerMcKesson Corporation dba SKY Packaging
Substance NameLABETALOL HYDROCHLORIDE
Strength200
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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