| NDC Code: |
52125-706 |
| Proprietary Name: |
Oxybutynin ChlorideExtended Release |
| Suffix: |
Extended Release |
| Non-Proprietary Name: |
Oxybutynin Chloride |
| Dosage Form: |
TABLET, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
19-09-2013 |
| Category Name: |
ANDA |
| Application Number: |
ANDA078503 |
| Labeler: |
REMEDYREPACK INC. |
| Substance Name: |
OXYBUTYNIN CHLORIDE |
| Active Numerator Strength: |
10 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
| DEA Schedule: |
|
