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"71335-9690-1" National Drug Code (NDC)

Labetalol Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (71335-9690-1)
(Bryant Ranch Prepack)

NDC Code71335-9690-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (71335-9690-1)
Product NDC71335-9690
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
Strength300
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-9690-1





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