"68001-206-03" National Drug Code (NDC)

Labetalol Hcl 500 TABLET, FILM COATED in 1 BOTTLE (68001-206-03)
(BluePoint Laboratories)

NDC Code68001-206-03
Package Description500 TABLET, FILM COATED in 1 BOTTLE (68001-206-03)
Product NDC68001-206
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hcl
Non-Proprietary NameLabetalol Hcl
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140226
End Marketing Date20210430
Marketing Category NameANDA
Application NumberANDA075113
ManufacturerBluePoint Laboratories
Substance NameLABETALOL HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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