"68462-211-03" National Drug Code (NDC)

Amlodipine Besylate 300 TABLET in 1 BOTTLE (68462-211-03)
(Glenmark Generics Inc., USA)

NDC Code68462-211-03
Package Description300 TABLET in 1 BOTTLE (68462-211-03)
Product NDC68462-211
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20090408
Marketing Category NameANDA
Application NumberANDA078552
ManufacturerGlenmark Generics Inc., USA
Substance NameAMLODIPINE BESYLATE
Strength5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

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