"70518-2289-0" National Drug Code (NDC)

Verapamil Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2289-0)
(REMEDYREPACK INC.)

NDC Code70518-2289-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2289-0)
Product NDC70518-2289
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVerapamil Hydrochloride
Non-Proprietary NameVerapamil Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190829
Marketing Category NameANDA
Application NumberANDA070995
ManufacturerREMEDYREPACK INC.
Substance NameVERAPAMIL HYDROCHLORIDE
Strength80
Strength Unitmg/1
Pharmacy ClassesP-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA]

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