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"71335-2359-5" National Drug Code (NDC)

Amlodipine Besylate 180 TABLET in 1 BOTTLE, PLASTIC (71335-2359-5)
(Bryant Ranch Prepack)

NDC Code71335-2359-5
Package Description180 TABLET in 1 BOTTLE, PLASTIC (71335-2359-5)
Product NDC71335-2359
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20190522
Marketing Category NameANDA
Application NumberANDA203245
ManufacturerBryant Ranch Prepack
Substance NameAMLODIPINE BESYLATE
Strength5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-2359-5





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