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"71930-037-52" National Drug Code (NDC)

Labetalol Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (71930-037-52)
(Eywa Pharma Inc)

NDC Code71930-037-52
Package Description500 TABLET, FILM COATED in 1 BOTTLE (71930-037-52)
Product NDC71930-037
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190524
Marketing Category NameANDA
Application NumberANDA207863
ManufacturerEywa 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/71930-037-52





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