"10135-719-20" National Drug Code (NDC)

Alendronate 2 BLISTER PACK in 1 CARTON (10135-719-20) / 10 TABLET in 1 BLISTER PACK
(Marlex Pharmaceuticals, Inc.)

NDC Code10135-719-20
Package Description2 BLISTER PACK in 1 CARTON (10135-719-20) / 10 TABLET in 1 BLISTER PACK
Product NDC10135-719
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
Strength70
Strength Unitmg/1
Pharmacy ClassesBisphosphonate [EPC], Diphosphonates [CS]

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