"59762-1530-3" National Drug Code (NDC)

Amlodipine Besylate 1000 TABLET in 1 BOTTLE (59762-1530-3)
(Greenstone LLC)

NDC Code59762-1530-3
Package Description1000 TABLET in 1 BOTTLE (59762-1530-3)
Product NDC59762-1530
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20070323
End Marketing Date20200331
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA019787
ManufacturerGreenstone LLC
Substance NameAMLODIPINE BESYLATE
Strength5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

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