"0093-7168-98" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE (0093-7168-98)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7168-98
Package Description90 TABLET in 1 BOTTLE (0093-7168-98)
Product NDC0093-7168
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20070710
End Marketing Date20191031
Marketing Category NameANDA
Application NumberANDA076846
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameAMLODIPINE BESYLATE
Strength10
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

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