Oxybutynin Chloride - Oxybutynin Chloride
Navigation: NDC > Supplier starting with: K > KREMERS URBAN PHARMACEUTICALS INC.| Field | Value |
|---|---|
| NDC Code: | 62175-272 |
| Proprietary Name: | Oxybutynin Chloride |
| Suffix: | Extended Release |
| Non-Proprietary Name: | Oxybutynin Chloride |
| Dosage Form: | TABLET, EXTENDED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 01-03-2009 |
| Category Name: | ANDA |
| Application Number: | ANDA078503 |
| Labeler: | KREMERS URBAN PHARMACEUTICALS INC. |
| Substance Name: | OXYBUTYNIN CHLORIDE |
| Active Numerator Strength: | 15 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
| DEA Schedule: |