"70677-0119-1" National Drug Code (NDC)

NDC Code	70677-0119-1
Package Description	1 BOTTLE in 1 CARTON (70677-0119-1) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC	70677-0119
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Sunmark Migraine Relief
Non-Proprietary Name	Acetaminophen, Aspirin, Caffeine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20200923
Marketing Category Name	ANDA
Application Number	ANDA075794
Manufacturer	Strategic Sourcing Services LLC
Substance Name	ACETAMINOPHEN; ASPIRIN; CAFFEINE
Strength	250; 250; 65
Strength Unit	mg/1; mg/1; mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]