"36800-969-20" National Drug Code (NDC)

NDC Code	36800-969-20
Package Description	200 TABLET, COATED in 1 BOTTLE, PLASTIC (36800-969-20)
Product NDC	36800-969
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Ibuprofen
Non-Proprietary Name	Ibuprofen
Dosage Form	TABLET, COATED
Usage	ORAL
Start Marketing Date	20191007
End Marketing Date	20220531
Marketing Category Name	ANDA
Application Number	ANDA079174
Manufacturer	TopCare
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]