"70934-751-60" National Drug Code (NDC)

Labetalol Hydrochloride 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-751-60)
(Denton Pharma, Inc. dba Northwind Pharmaceuticals)

NDC Code70934-751-60
Package Description60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-751-60)
Product NDC70934-751
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200528
Marketing Category NameANDA
Application NumberANDA207863
ManufacturerDenton Pharma, Inc. dba Northwind Pharmaceuticals
Substance NameLABETALOL HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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