"47335-636-08" National Drug Code (NDC)

Alendronate Sodium 100 TABLET in 1 BOTTLE (47335-636-08)
(Sun Pharma Global FZE)

NDC Code47335-636-08
Package Description100 TABLET in 1 BOTTLE (47335-636-08)
Product NDC47335-636
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
Strength10
Strength Unitmg/1
Pharmacy ClassesBisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

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