"70069-746-25" National Drug Code (NDC)

NDC Code	70069-746-25
Package Description	25 BOTTLE in 1 CARTON (70069-746-25) / 5 mL in 1 BOTTLE
Product NDC	70069-746
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potassium Phosphate
Non-Proprietary Name	Potassium Phosphate
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20240711
Marketing Category Name	ANDA
Application Number	ANDA217726
Manufacturer	Somerset Therapeutics, LLC
Substance Name	DIBASIC POTASSIUM PHOSPHATE; MONOBASIC POTASSIUM PHOSPHATE
Strength	236; 224
Strength Unit	mg/mL; mg/mL
Pharmacy Classes	Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Compounds [CS], Potassium Salt [EPC], Potassium Salt [EPC]