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"47335-635-18" National Drug Code (NDC)

Alendronate Sodium 1000 TABLET in 1 BOTTLE (47335-635-18)
(Sun Pharma Global FZE)

NDC Code47335-635-18
Package Description1000 TABLET in 1 BOTTLE (47335-635-18)
Product NDC47335-635
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlendronate Sodium
Non-Proprietary NameAlendronate Sodium
Dosage FormTABLET
UsageORAL
Start Marketing Date20141215
Marketing Category NameANDA
Application NumberANDA090022
ManufacturerSun Pharma Global FZE
Substance NameALENDRONATE SODIUM
Strength5
Strength Unitmg/1
Pharmacy ClassesBisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/47335-635-18





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