"0603-2108-21" National Drug Code (NDC)

Amlodipine Besylate 100 TABLET in 1 BOTTLE, PLASTIC (0603-2108-21)
(Qualitest Pharmaceuticals)

NDC Code0603-2108-21
Package Description100 TABLET in 1 BOTTLE, PLASTIC (0603-2108-21)
Product NDC0603-2108
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20100407
Marketing Category NameANDA
Application NumberANDA078414
ManufacturerQualitest Pharmaceuticals
Substance NameAMLODIPINE BESYLATE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

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