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) |
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 NDC: | 0603-1491-54 |
Package Description: | 118 mL in 1 BOTTLE (0603-1491-54) |
NDC Code | 0603-1491-54 |
Proprietary Name | Oxybutynin Chloride |
Package Description | 118 mL in 1 BOTTLE (0603-1491-54) |
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] |