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"72162-2121-1" National Drug Code (NDC)
Potassium Citrate 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2121-1)
(Bryant Ranch Prepack)
NDC Code
72162-2121-1
Package Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2121-1)
Product NDC
72162-2121
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
20210215
Marketing Category Name
ANDA
Application Number
ANDA214420
Manufacturer
Bryant Ranch Prepack
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/72162-2121-1