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"50090-6778-0" National Drug Code (NDC)

Labetalol Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (50090-6778-0)
(A-S Medication Solutions)

NDC Code50090-6778-0
Package Description90 TABLET, FILM COATED in 1 BOTTLE (50090-6778-0)
Product NDC50090-6778
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19980803
Marketing Category NameANDA
Application NumberANDA075133
ManufacturerA-S Medication Solutions
Substance NameLABETALOL HYDROCHLORIDE
Strength200
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50090-6778-0





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