"64679-421-02" National Drug Code (NDC)

Amlodipine Besylate 1000 TABLET in 1 BOTTLE (64679-421-02)
(Wockhardt USA LLC.)

NDC Code64679-421-02
Package Description1000 TABLET in 1 BOTTLE (64679-421-02)
Product NDC64679-421
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20070906
Marketing Category NameANDA
Application NumberANDA078500
ManufacturerWockhardt USA LLC.
Substance NameAMLODIPINE BESYLATE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

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