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Ascomp with Codeine
Ascomp with Codeine - 51991-074-05 - (Butalbital, Aspirin, Caffeine and Codeine Phosphate)
Drug Information of Ascomp with Codeine
| Product NDC: | 51991-074 |
| Proprietary Name: | Ascomp with Codeine |
| Non Proprietary Name: | Butalbital, Aspirin, Caffeine and Codeine Phosphate |
| Active Ingredient(s): | 325; 50; 40; 30 mg/1; mg/1; mg/1; mg/1 & nbsp; Butalbital, Aspirin, Caffeine and Codeine Phosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ascomp with Codeine
| Product NDC: | 51991-074 |
| Labeler Name: | Breckenridge Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075231 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090501 |
Package Information of Ascomp with Codeine
| Package NDC: | 51991-074-05 |
| Package Description: | 500 CAPSULE in 1 BOTTLE, PLASTIC (51991-074-05) |
NDC Information of Ascomp with Codeine
| NDC Code | 51991-074-05 |
| Proprietary Name | Ascomp with Codeine |
| Package Description | 500 CAPSULE in 1 BOTTLE, PLASTIC (51991-074-05) |
| Product NDC | 51991-074 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Butalbital, Aspirin, Caffeine and Codeine Phosphate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20090501 |
| Marketing Category Name | ANDA |
| Labeler Name | Breckenridge Pharmaceutical, Inc. |
| Substance Name | ASPIRIN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE |
| Strength Number | 325; 50; 40; 30 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes | Barbiturate [EPC],Barbiturates [Chemical/Ingredient],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] |
