Oxybutynin Chloride - oxybutynin chloride
Navigation: NDC > Supplier starting with: U > UDL LABORATORIES, INC.| Field | Value |
|---|---|
| NDC Code: | 51079-722 |
| Proprietary Name: | Oxybutynin Chloride |
| Suffix: | |
| Non-Proprietary Name: | oxybutynin chloride |
| Dosage Form: | TABLET, FILM COATED, EXTENDED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 14-01-2011 |
| Category Name: | ANDA |
| Application Number: | ANDA076702 |
| Labeler: | UDL LABORATORIES, INC. |
| Substance Name: | OXYBUTYNIN CHLORIDE |
| Active Numerator Strength: | 5 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
| DEA Schedule: |