"51862-135-30" National Drug Code (NDC)

NDC Code	51862-135-30
Package Description	30 POUCH in 1 CARTON (51862-135-30) > 1.83 g in 1 POUCH (51862-135-02)
Product NDC	51862-135
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potassium Chloride
Non-Proprietary Name	Potassium Chloride
Dosage Form	POWDER
Usage	ORAL
Start Marketing Date	20150316
End Marketing Date	20200430
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Mayne Pharma Inc.
Substance Name	POTASSIUM CHLORIDE
Strength	20
Strength Unit	meq/1.5g
Pharmacy Classes	Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]