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"60723-205-32" National Drug Code (NDC)

Alendronate 3 BLISTER PACK in 1 CARTON (60723-205-32) / 4 TABLET in 1 BLISTER PACK
(Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd.)

NDC Code60723-205-32
Package Description3 BLISTER PACK in 1 CARTON (60723-205-32) / 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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/60723-205-32





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