| NDC Code | 16571-768-09 |
|---|
| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16571-768-09) |
|---|
| Product NDC | 16571-768 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Darifenacin |
|---|
| Non-Proprietary Name | Darifenacin |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20160919 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA206743 |
|---|
| Manufacturer | Rising Pharma Holdings, Inc. |
|---|
| Substance Name | DARIFENACIN HYDROBROMIDE |
|---|
| Strength | 15 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] |
|---|