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"0093-5172-29" National Drug Code (NDC)

Alendronate Sodium 12 BLISTER PACK in 1 PACKAGE (0093-5172-29) > 1 TABLET in 1 BLISTER PACK (0093-5172-19)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-5172-29
Package Description12 BLISTER PACK in 1 PACKAGE (0093-5172-29) > 1 TABLET in 1 BLISTER PACK (0093-5172-19)
Product NDC0093-5172
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlendronate Sodium
Non-Proprietary NameAlendronate Sodium
Dosage FormTABLET
UsageORAL
Start Marketing Date20080206
End Marketing Date20171231
Marketing Category NameANDA
Application NumberANDA075710
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameALENDRONATE SODIUM
Strength35
Strength Unitmg/1
Pharmacy ClassesBisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-5172-29





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