"50090-7001-1" National Drug Code (NDC)

Labetalol Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (50090-7001-1)
(A-S Medication Solutions)

NDC Code50090-7001-1
Package Description90 TABLET, FILM COATED in 1 BOTTLE (50090-7001-1)
Product NDC50090-7001
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210208
Marketing Category NameANDA
Application NumberANDA075215
ManufacturerA-S Medication Solutions
Substance NameLABETALOL HYDROCHLORIDE
Strength200
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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