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"68382-538-05" National Drug Code (NDC)
Potassium Citrate 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-538-05)
(Zydus Pharmaceuticals (USA) Inc.)
NDC Code
68382-538-05
Package Description
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-538-05)
Product NDC
68382-538
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Potassium Citrate
Non-Proprietary Name
Potassium Citrate
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20140812
Marketing Category Name
ANDA
Application Number
ANDA203546
Manufacturer
Zydus Pharmaceuticals (USA) Inc.
Substance Name
POTASSIUM CITRATE
Strength
15
Strength Unit
meq/1
Pharmacy Classes
Acidifying 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/68382-538-05