"47682-610-33" National Drug Code (NDC)

NDC Code	47682-610-33
Package Description	50 PACKET in 1 BOX (47682-610-33) / 2 TABLET, COATED in 1 PACKET (47682-610-99)
Product NDC	47682-610
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Green Guard Ibupro Relief
Non-Proprietary Name	Ibuprofen
Dosage Form	TABLET, COATED
Usage	ORAL
Start Marketing Date	20160201
Marketing Category Name	ANDA
Application Number	ANDA075010
Manufacturer	Unifirst First Aid Corporation
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]