Duloxetine - Duloxetine
Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL FZE| Field | Value |
|---|---|
| NDC Code: | 47335-381 |
| Proprietary Name: | Duloxetine |
| Suffix: | |
| Non-Proprietary Name: | Duloxetine |
| Dosage Form: | CAPSULE, DELAYED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 11-12-2013 |
| Category Name: | ANDA |
| Application Number: | ANDA090745 |
| Labeler: | SUN PHARMA GLOBAL FZE |
| Substance Name: | DULOXETINE HYDROCHLORIDE |
| Active Numerator Strength: | 20 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
| DEA Schedule: |