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"69452-193-30" National Drug Code (NDC)

Potassium Citrate 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69452-193-30)
(Bionpharma Inc.)

NDC Code69452-193-30
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69452-193-30)
Product NDC69452-193
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePotassium Citrate
Non-Proprietary NamePotassium Citrate
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20191214
Marketing Category NameANDA
Application NumberANDA212799
ManufacturerBionpharma Inc.
Substance NamePOTASSIUM CITRATE
Strength10
Strength Unitmeq/1
Pharmacy ClassesAcidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69452-193-30





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