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"60290-056-03" National Drug Code (NDC)

Ranolazine 6 BLISTER PACK in 1 CARTON (60290-056-03) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(Umedica Laboratories USA Inc.)

NDC Code60290-056-03
Package Description6 BLISTER PACK in 1 CARTON (60290-056-03) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC60290-056
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanolazine
Non-Proprietary NameRanolazine
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20260810
Marketing Category NameANDA
Application NumberANDA214551
ManufacturerUmedica Laboratories USA Inc.
Substance NameRANOLAZINE
Strength1000
Strength Unitmg/1
Pharmacy ClassesAnti-anginal [EPC], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]

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