"71335-1318-1" National Drug Code (NDC)

Felodipine 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1318-1)
(Bryant Ranch Prepack)

NDC Code71335-1318-1
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1318-1)
Product NDC71335-1318
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFelodipine
Non-Proprietary NameFelodipine
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20130117
Marketing Category NameANDA
Application NumberANDA203417
ManufacturerBryant Ranch Prepack
Substance NameFELODIPINE
Strength5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-1318-1