| NDC Code | 68382-257-01 |
|---|
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-257-01) |
|---|
| Product NDC | 68382-257 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Oxybutynin |
|---|
| Non-Proprietary Name | Oxybutynin |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20170810 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202332 |
|---|
| Manufacturer | Zydus Pharmaceuticals USA Inc. |
|---|
| Substance Name | OXYBUTYNIN CHLORIDE |
|---|
| Strength | 15 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] |
|---|