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"71335-2169-2" National Drug Code (NDC)

Labetalol Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (71335-2169-2)
(Bryant Ranch Prepack)

NDC Code71335-2169-2
Package Description90 TABLET, FILM COATED in 1 BOTTLE (71335-2169-2)
Product NDC71335-2169
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210818
Marketing Category NameANDA
Application NumberANDA211953
ManufacturerBryant Ranch Prepack
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/71335-2169-2





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