"0093-5141-01" National Drug Code (NDC)

Alendronate Sodium 100 TABLET in 1 BOTTLE (0093-5141-01)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-5141-01
Package Description100 TABLET in 1 BOTTLE (0093-5141-01)
Product NDC0093-5141
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlendronate Sodium
Non-Proprietary NameAlendronate Sodium
Dosage FormTABLET
UsageORAL
Start Marketing Date20080206
End Marketing Date20180531
Marketing Category NameANDA
Application NumberANDA075710
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameALENDRONATE SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesBisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

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