Fluoxetine - FLUOXETINE HYDROCHLORIDE
Navigation: NDC > Supplier starting with: P > PHARMACEUTICAL ASSOCIATES, INC.| Field | Value |
|---|---|
| NDC Code: | 0121-0721 |
| Proprietary Name: | Fluoxetine |
| Suffix: | |
| Non-Proprietary Name: | FLUOXETINE HYDROCHLORIDE |
| Dosage Form: | SOLUTION |
| Method: | ORAL |
| Original Marketing Date: | 30-01-2002 |
| Category Name: | ANDA |
| Application Number: | ANDA076015 |
| Labeler: | PHARMACEUTICAL ASSOCIATES, INC. |
| Substance Name: | FLUOXETINE HYDROCHLORIDE |
| Active Numerator Strength: | 20 |
| Active Ingredient Unit: | mg/5mL |
| Pharm Classes: | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
| DEA Schedule: |