"71335-1032-4" National Drug Code (NDC)

Amlodipine Besylate 300 TABLET in 1 BOTTLE (71335-1032-4)
(Bryant Ranch Prepack)

NDC Code71335-1032-4
Package Description300 TABLET in 1 BOTTLE (71335-1032-4)
Product NDC71335-1032
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20071102
Marketing Category NameANDA
Application NumberANDA077955
ManufacturerBryant Ranch Prepack
Substance NameAMLODIPINE BESYLATE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

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