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"68001-700-03" National Drug Code (NDC)

Labetalol Hydrochloride 500 TABLET in 1 BOTTLE (68001-700-03)
(BluePoint Laboratories)

NDC Code68001-700-03
Package Description500 TABLET in 1 BOTTLE (68001-700-03)
Product NDC68001-700
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20260315
Marketing Category NameANDA
Application NumberANDA074787
ManufacturerBluePoint Laboratories
Substance NameLABETALOL HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68001-700-03





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