"21695-726-30" National Drug Code (NDC)

NDC Code	21695-726-30
Package Description	30 TABLET, MULTILAYER in 1 BOTTLE (21695-726-30)
Product NDC	21695-726
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Orphenadrine Citrate, Aspirin And Caffeine
Non-Proprietary Name	Orphenadrine Citrate, Aspirin And Caffeine
Dosage Form	TABLET, MULTILAYER
Usage	ORAL
Start Marketing Date	19961231
Marketing Category Name	ANDA
Application Number	ANDA074654
Manufacturer	Rebel Distributors Corp
Substance Name	ORPHENADRINE CITRATE; ASPIRIN; CAFFEINE
Strength	50; 770; 60
Strength Unit	mg/1; mg/1; mg/1
Pharmacy Classes	Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC],Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC],Platelet Aggregation Inhibitor [EPC],Decreased Platelet Aggregation [PE],Central Nervous System Stimulant [EPC],Methylxanthine [EPC],Xanthines [CS],Central Nervous System Stimulation [PE]