"59779-050-82" National Drug Code (NDC)

NDC Code	59779-050-82
Package Description	200 TABLET, FILM COATED in 1 BOTTLE (59779-050-82)
Product NDC	59779-050
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Ibuprofen Pm
Non-Proprietary Name	Diphenhydramine Citrate And Ibuprofen
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20090217
Marketing Category Name	ANDA
Application Number	ANDA079113
Manufacturer	CVS Pharmacy
Substance Name	DIPHENHYDRAMINE CITRATE; IBUPROFEN
Strength	38; 200
Strength Unit	mg/1; mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]