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"59762-1520-2" National Drug Code (NDC)

Amlodipine Besylate 300 TABLET in 1 BOTTLE (59762-1520-2)
(Greenstone LLC)

NDC Code59762-1520-2
Package Description300 TABLET in 1 BOTTLE (59762-1520-2)
Product NDC59762-1520
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
Strength2.5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59762-1520-2





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