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"51655-322-25" National Drug Code (NDC)

Labetalol Hydrochloride 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-322-25)
(Northwind Pharmaceuticals, LLC)

NDC Code51655-322-25
Package Description60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-322-25)
Product NDC51655-322
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20230425
Marketing Category NameANDA
Application NumberANDA209603
ManufacturerNorthwind Pharmaceuticals, LLC
Substance NameLABETALOL HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51655-322-25





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