"60723-205-31" National Drug Code (NDC)

Alendronate 1 BLISTER PACK in 1 CARTON (60723-205-31) / 4 TABLET in 1 BLISTER PACK
(Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd.)

NDC Code60723-205-31
Package Description1 BLISTER PACK in 1 CARTON (60723-205-31) / 4 TABLET in 1 BLISTER PACK
Product NDC60723-205
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlendronate
Non-Proprietary NameAlendronate Sodium
Dosage FormTABLET
UsageORAL
Start Marketing Date20171205
Marketing Category NameANDA
Application NumberANDA090258
ManufacturerHangzhou Minsheng Binjiang Pharmaceutical Co., Ltd.
Substance NameALENDRONATE SODIUM
Strength70
Strength Unitmg/1
Pharmacy ClassesBisphosphonate [EPC], Diphosphonates [CS]

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