"21695-570-30" National Drug Code (NDC)

NDC Code	21695-570-30
Package Description	30 TABLET in 1 BOTTLE (21695-570-30)
Product NDC	21695-570
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carisoprodol And Aspirin
Non-Proprietary Name	Carisoprodol And Aspirin
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20091001
Marketing Category Name	ANDA
Application Number	ANDA040116
Manufacturer	Rebel Distributors Corp
Substance Name	CARISOPRODOL; ASPIRIN
Strength	200; 325
Strength Unit	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]