"10135-697-12" National Drug Code (NDC)

Alendronate 3 BLISTER PACK in 1 CARTON (10135-697-12) > 4 TABLET in 1 BLISTER PACK
(Marlex Pharmaceuticals Inc)

NDC Code10135-697-12
Package Description3 BLISTER PACK in 1 CARTON (10135-697-12) > 4 TABLET in 1 BLISTER PACK
Product NDC10135-697
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlendronate
Non-Proprietary NameAlendronate Sodium
Dosage FormTABLET
UsageORAL
Start Marketing Date20200301
Marketing Category NameANDA
Application NumberANDA090258
ManufacturerMarlex Pharmaceuticals Inc
Substance NameALENDRONATE SODIUM
Strength70
Strength Unitmg/1
Pharmacy ClassesBisphosphonate [EPC],Diphosphonates [CS]

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