"71085-083-30" National Drug Code (NDC)

NDC Code	71085-083-30
Package Description	30 POUCH in 1 CARTON (71085-083-30) / 3.16 g in 1 POUCH (71085-083-01)
Product NDC	71085-083
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potassium Chloride
Non-Proprietary Name	Potassium Chloride
Dosage Form	FOR SOLUTION
Usage	ORAL
Start Marketing Date	20251201
End Marketing Date	20281130
Marketing Category Name	NDA
Application Number	NDA208019
Manufacturer	IPG Pharmaceuticals, Inc.
Substance Name	POTASSIUM CHLORIDE
Strength	3
Strength Unit	g/3.16g
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]