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"68001-382-03" National Drug Code (NDC)

Labetalol Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (68001-382-03)
(BluePoint Laboratories Inc.)

NDC Code68001-382-03
Package Description500 TABLET, FILM COATED in 1 BOTTLE (68001-382-03)
Product NDC68001-382
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190218
Marketing Category NameANDA
Application NumberANDA207743
ManufacturerBluePoint Laboratories Inc.
Substance NameLABETALOL HYDROCHLORIDE
Strength200
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68001-382-03





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