"0093-7029-98" National Drug Code (NDC)

Amlodipine And Olmesartan Medoxomil 90 TABLET, FILM COATED in 1 BOTTLE (0093-7029-98)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7029-98
Package Description90 TABLET, FILM COATED in 1 BOTTLE (0093-7029-98)
Product NDC0093-7029
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine And Olmesartan Medoxomil
Non-Proprietary NameAmlodipine And Olmesartan Medoxomil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20161026
End Marketing Date20200430
Marketing Category NameANDA
Application NumberANDA091154
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameAMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
Strength10; 20
Strength Unitmg/1; mg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

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