Product NDC: | 0832-0510 |
Proprietary Name: | Bethanechol Chloride |
Non Proprietary Name: | Bethanechol Chloride |
Active Ingredient(s): | 5 mg/1 & nbsp; Bethanechol Chloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0832-0510 |
Labeler Name: | Upsher-Smith Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040633 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100124 |
Package NDC: | 0832-0510-01 |
Package Description: | 10 BLISTER PACK in 1 CARTON (0832-0510-01) > 10 TABLET in 1 BLISTER PACK (0832-0510-89) |
NDC Code | 0832-0510-01 |
Proprietary Name | Bethanechol Chloride |
Package Description | 10 BLISTER PACK in 1 CARTON (0832-0510-01) > 10 TABLET in 1 BLISTER PACK (0832-0510-89) |
Product NDC | 0832-0510 |
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 | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cholinergic Muscarinic Agonist [EPC],Cholinergic Muscarinic Agonists [MoA] |