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"68382-536-05" National Drug Code (NDC)

Potassium Citrate 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-536-05)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code68382-536-05
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-536-05)
Product NDC68382-536
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePotassium Citrate
Non-Proprietary NamePotassium Citrate
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20140812
Marketing Category NameANDA
Application NumberANDA203546
ManufacturerZydus Pharmaceuticals (USA) Inc.
Substance NamePOTASSIUM CITRATE
Strength5
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/68382-536-05





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