| Product NDC: | 67877-186 | 
| Proprietary Name: | CHLORDIAZEPOXIDE HYDROCHLORIDE and CLIDINIUM BROMIDE | 
| Non Proprietary Name: | CHLORDIAZEPOXIDE HYDROCHLORIDE and CLIDINIUM BROMIDE | 
| Active Ingredient(s): | 5; 2.5 mg/1; mg/1 & nbsp; CHLORDIAZEPOXIDE HYDROCHLORIDE and CLIDINIUM BROMIDE | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | CAPSULE | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 67877-186 | 
| Labeler Name: | Ascend Laboratories, LLC | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER | 
| Start Marketing Date: | 20100122 | 
| Package NDC: | 67877-186-01 | 
| Package Description: | 100 CAPSULE in 1 BOTTLE (67877-186-01) | 
| NDC Code | 67877-186-01 | 
| Proprietary Name | CHLORDIAZEPOXIDE HYDROCHLORIDE and CLIDINIUM BROMIDE | 
| Package Description | 100 CAPSULE in 1 BOTTLE (67877-186-01) | 
| Product NDC | 67877-186 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | CHLORDIAZEPOXIDE HYDROCHLORIDE and CLIDINIUM BROMIDE | 
| Dosage Form Name | CAPSULE | 
| Route Name | ORAL | 
| Start Marketing Date | 20100122 | 
| Marketing Category Name | UNAPPROVED DRUG OTHER | 
| Labeler Name | Ascend Laboratories, LLC | 
| Substance Name | CHLORDIAZEPOXIDE HYDROCHLORIDE; CLIDINIUM BROMIDE | 
| Strength Number | 5; 2.5 | 
| Strength Unit | mg/1; mg/1 | 
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient],Anticholinergic [EPC],Decreased Parasympathetic Acetylcholine Activity [PE],GI Motility Alteration [PE],Digestive/GI System Activity Alteration [PE],Cholinergic Antagonists [MoA] |