Home
>
National Drug Code (NDC)
>
Oxybutynin Chloride
Oxybutynin Chloride - 0603-1491-58 - (oxybutynin chloride)
Drug Information of Oxybutynin Chloride
| Product NDC: | 0603-1491 |
| Proprietary Name: | Oxybutynin Chloride |
| Non Proprietary Name: | oxybutynin chloride |
| Active Ingredient(s): | 5 mg/5mL & nbsp; oxybutynin chloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxybutynin Chloride
| Product NDC: | 0603-1491 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076682 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20041228 |
Package Information of Oxybutynin Chloride
| Package NDC: | 0603-1491-58 |
| Package Description: | 473 mL in 1 BOTTLE (0603-1491-58) |
NDC Information of Oxybutynin Chloride
| NDC Code | 0603-1491-58 |
| Proprietary Name | Oxybutynin Chloride |
| Package Description | 473 mL in 1 BOTTLE (0603-1491-58) |
| Product NDC | 0603-1491 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxybutynin chloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20041228 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | OXYBUTYNIN CHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
