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"71335-1761-5" National Drug Code (NDC)

Amlodipine Besylate 500 TABLET in 1 BOTTLE (71335-1761-5)
(Bryant Ranch Prepack)

NDC Code71335-1761-5
Package Description500 TABLET in 1 BOTTLE (71335-1761-5)
Product NDC71335-1761
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20140303
End Marketing Date20230501
Marketing Category NameANDA
Application NumberANDA203245
ManufacturerBryant Ranch Prepack
Substance NameAMLODIPINE BESYLATE
Strength2.5
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/71335-1761-5





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