"69367-265-01" National Drug Code (NDC)

Felodipine 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-265-01)
(Westminster Pharmaceuticals, LLC)

NDC Code69367-265-01
Package Description100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-265-01)
Product NDC69367-265
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFelodipine
Non-Proprietary NameFelodipine
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20230331
Marketing Category NameANDA
Application NumberANDA210847
ManufacturerWestminster Pharmaceuticals, LLC
Substance NameFELODIPINE
Strength5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

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