"61786-393-02" National Drug Code (NDC)

Labetalol Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (61786-393-02)
(REMEDYREPACK INC.)

NDC Code61786-393-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (61786-393-02)
Product NDC61786-393
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150812
Marketing Category NameANDA
Application NumberANDA075133
ManufacturerREMEDYREPACK INC.
Substance NameLABETALOL HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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