"31722-300-32" National Drug Code (NDC)

NDC Code	31722-300-32
Package Description	1 CARTON in 1 KIT (31722-300-32) / 30 PACKET in 1 CARTON (31722-300-31) / 1 POWDER, FOR SUSPENSION in 1 PACKET (31722-300-12)
Product NDC	31722-300
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Eltrombopag
Non-Proprietary Name	Eltrombopag Olamine
Dosage Form	POWDER, FOR SUSPENSION
Usage	ORAL
Start Marketing Date	20250513
Marketing Category Name	ANDA
Application Number	ANDA216620
Manufacturer	Camber Pharmaceuticals, Inc.
Substance Name	ELTROMBOPAG OLAMINE
Strength	12.5
Strength Unit	mg/1
Pharmacy Classes	Breast Cancer Resistance Protein Inhibitors [MoA], Increased Megakaryocyte Maturation [PE], Increased Platelet Production [PE], Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA], Thrombopoietin Receptor Agonist [EPC], Thrombopoietin Receptor Agonists [MoA], UGT1A1 Inhibitors [MoA], UGT1A3 Inhibitors [MoA], UGT1A4 Inhibitors [MoA], UGT1A6 Inhibitors [MoA], UGT1A9 Inhibitors [MoA], UGT2B15 Inhibitors [MoA], UGT2B7 Inhibitors [MoA]