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"53002-2034-3" National Drug Code (NDC)
Potassium Chloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (53002-2034-3)
(RPK Pharmaceuticals, Inc.)
NDC Code
53002-2034-3
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (53002-2034-3)
Product NDC
53002-2034
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Potassium Chloride
Non-Proprietary Name
Potassium Chloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20181127
Marketing Category Name
ANDA
Application Number
ANDA210733
Manufacturer
RPK Pharmaceuticals, Inc.
Substance Name
POTASSIUM CHLORIDE
Strength
750
Strength Unit
mg/1
Pharmacy Classes
Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/53002-2034-3