"10135-696-12" National Drug Code (NDC)

Alendronate 3 BLISTER PACK in 1 CARTON (10135-696-12) > 4 TABLET in 1 BLISTER PACK
(Marlex Pharmaceuticals Inc)

NDC Code10135-696-12
Package Description3 BLISTER PACK in 1 CARTON (10135-696-12) > 4 TABLET in 1 BLISTER PACK
Product NDC10135-696
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
Strength35
Strength Unitmg/1
Pharmacy ClassesBisphosphonate [EPC],Diphosphonates [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/10135-696-12