Product NDC: | 21695-726 |
Proprietary Name: | Orphenadrine Citrate, Aspirin and Caffeine |
Non Proprietary Name: | Orphenadrine Citrate, Aspirin and Caffeine |
Active Ingredient(s): | 770; 60; 50 mg/1; mg/1; mg/1 & nbsp; Orphenadrine Citrate, Aspirin and Caffeine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, MULTILAYER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-726 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074654 |
Marketing Category: | ANDA |
Start Marketing Date: | 19961231 |
Package NDC: | 21695-726-45 |
Package Description: | 45 TABLET, MULTILAYER in 1 BOTTLE (21695-726-45) |
NDC Code | 21695-726-45 |
Proprietary Name | Orphenadrine Citrate, Aspirin and Caffeine |
Package Description | 45 TABLET, MULTILAYER in 1 BOTTLE (21695-726-45) |
Product NDC | 21695-726 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Orphenadrine Citrate, Aspirin and Caffeine |
Dosage Form Name | TABLET, MULTILAYER |
Route Name | ORAL |
Start Marketing Date | 19961231 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | ASPIRIN; CAFFEINE; ORPHENADRINE CITRATE |
Strength Number | 770; 60; 50 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical 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],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |