"0185-0117-01" National Drug Code (NDC)

Labetalol Hcl 100 TABLET, FILM COATED in 1 BOTTLE (0185-0117-01)
(Eon Labs, Inc.)

NDC Code0185-0117-01
Package Description100 TABLET, FILM COATED in 1 BOTTLE (0185-0117-01)
Product NDC0185-0117
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hcl
Non-Proprietary NameLabetalol Hcl
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19980804
End Marketing Date20230930
Marketing Category NameANDA
Application NumberANDA075113
ManufacturerEon Labs, Inc.
Substance NameLABETALOL HYDROCHLORIDE
Strength200
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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