"0603-2109-02" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE, PLASTIC (0603-2109-02)
(Par Pharmaceutical)

NDC Code0603-2109-02
Package Description90 TABLET in 1 BOTTLE, PLASTIC (0603-2109-02)
Product NDC0603-2109
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20100407
End Marketing Date20190630
Marketing Category NameANDA
Application NumberANDA078414
ManufacturerPar Pharmaceutical
Substance NameAMLODIPINE BESYLATE
Strength5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

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