| Product NDC: | 0832-0511 | 
| Proprietary Name: | Bethanechol Chloride | 
| Non Proprietary Name: | Bethanechol Chloride | 
| Active Ingredient(s): | 10 mg/1 & nbsp; Bethanechol Chloride | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0832-0511 | 
| Labeler Name: | Upsher-Smith Laboratories, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA040634 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20100124 | 
| Package NDC: | 0832-0511-01 | 
| Package Description: | 10 BLISTER PACK in 1 CARTON (0832-0511-01) > 10 TABLET in 1 BLISTER PACK (0832-0511-89) | 
| NDC Code | 0832-0511-01 | 
| Proprietary Name | Bethanechol Chloride | 
| Package Description | 10 BLISTER PACK in 1 CARTON (0832-0511-01) > 10 TABLET in 1 BLISTER PACK (0832-0511-89) | 
| Product NDC | 0832-0511 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Bethanechol Chloride | 
| Dosage Form Name | TABLET | 
| Route Name | ORAL | 
| Start Marketing Date | 20100124 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Upsher-Smith Laboratories, Inc. | 
| Substance Name | BETHANECHOL CHLORIDE | 
| Strength Number | 10 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Cholinergic Muscarinic Agonist [EPC],Cholinergic Muscarinic Agonists [MoA] |