"72090-002-01" National Drug Code (NDC)

NDC Code	72090-002-01
Package Description	500 TABLET in 1 BOTTLE (72090-002-01)
Product NDC	72090-002
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Pain Reliever / Fever Reducer
Non-Proprietary Name	Ibuprofen
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20210518
Marketing Category Name	OTC MONOGRAPH NOT FINAL
Application Number	part343
Manufacturer	Pioneer Life Sciences, LLC
Substance Name	IBUPROFEN
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]