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"10135-718-12" National Drug Code (NDC)

Alendronate 3 BLISTER PACK in 1 CARTON (10135-718-12) / 4 TABLET in 1 BLISTER PACK
(Marlex Pharmaceuticals, Inc.)

NDC Code10135-718-12
Package Description3 BLISTER PACK in 1 CARTON (10135-718-12) / 4 TABLET in 1 BLISTER PACK
Product NDC10135-718
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlendronate
Non-Proprietary NameAlendronate Sodium Tablet
Dosage FormTABLET
UsageORAL
Start Marketing Date20201201
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/10135-718-12





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