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"70377-062-13" National Drug Code (NDC)

Labetalol Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (70377-062-13)
(Biocon Pharma Inc.)

NDC Code70377-062-13
Package Description500 TABLET, FILM COATED in 1 BOTTLE (70377-062-13)
Product NDC70377-062
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210527
Marketing Category NameANDA
Application NumberANDA209603
ManufacturerBiocon Pharma Inc.
Substance NameLABETALOL HYDROCHLORIDE
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/70377-062-13





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