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"51655-869-83" National Drug Code (NDC)

Amlodipine Besylate 180 TABLET in 1 BOTTLE, PLASTIC (51655-869-83)
(Northwind Pharmaceuticals, LLC)

NDC Code51655-869-83
Package Description180 TABLET in 1 BOTTLE, PLASTIC (51655-869-83)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51655-869-83





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