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"71335-2057-2" National Drug Code (NDC)

Labetalol Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (71335-2057-2)
(Bryant Ranch Prepack)

NDC Code71335-2057-2
Package Description90 TABLET, FILM COATED in 1 BOTTLE (71335-2057-2)
Product NDC71335-2057
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20191122
Marketing Category NameANDA
Application NumberANDA075215
ManufacturerBryant Ranch Prepack
Substance NameLABETALOL
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/71335-2057-2





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