Product NDC: | 64679-967 |
Proprietary Name: | Bethanechol Chloride |
Non Proprietary Name: | Bethanechol Chloride 25 mg |
Active Ingredient(s): | 25 mg/1 & nbsp; Bethanechol Chloride 25 mg |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64679-967 |
Labeler Name: | Wockhardt USA LLC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040534 |
Marketing Category: | ANDA |
Start Marketing Date: | 20030929 |
Package NDC: | 64679-967-01 |
Package Description: | 100 TABLET in 1 BOTTLE (64679-967-01) |
NDC Code | 64679-967-01 |
Proprietary Name | Bethanechol Chloride |
Package Description | 100 TABLET in 1 BOTTLE (64679-967-01) |
Product NDC | 64679-967 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Bethanechol Chloride 25 mg |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20030929 |
Marketing Category Name | ANDA |
Labeler Name | Wockhardt USA LLC. |
Substance Name | BETHANECHOL CHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cholinergic Muscarinic Agonist [EPC],Cholinergic Muscarinic Agonists [MoA] |