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"70518-1132-0" National Drug Code (NDC)

Labetalol Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1132-0)
(REMEDYREPACK INC.)

NDC Code70518-1132-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1132-0)
Product NDC70518-1132
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180424
Marketing Category NameANDA
Application NumberANDA207743
ManufacturerREMEDYREPACK INC.
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/70518-1132-0





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