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"52125-257-02" National Drug Code (NDC)

Labetalol Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-257-02)
(REMEDYREPACK INC.)

NDC Code52125-257-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (52125-257-02)
Product NDC52125-257
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20121008
Marketing Category NameANDA
Application NumberANDA075133
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/52125-257-02





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