"51655-869-52" National Drug Code (NDC)

Amlodipine Besylate 30 TABLET in 1 BOTTLE, PLASTIC (51655-869-52)
(Northwind Pharmaceuticals, LLC)

NDC Code51655-869-52
Package Description30 TABLET in 1 BOTTLE, PLASTIC (51655-869-52)
Product NDC51655-869
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20230825
Marketing Category NameANDA
Application NumberANDA077073
ManufacturerNorthwind Pharmaceuticals, LLC
Substance NameAMLODIPINE BESYLATE
Strength10
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

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