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"0093-7167-55" National Drug Code (NDC)

Amlodipine Besylate 300 TABLET in 1 BOTTLE (0093-7167-55)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7167-55
Package Description300 TABLET in 1 BOTTLE (0093-7167-55)
Product NDC0093-7167
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20070710
End Marketing Date20190630
Marketing Category NameANDA
Application NumberANDA076846
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameAMLODIPINE BESYLATE
Strength5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-7167-55





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