Fluoxetine Hydrochloride - fluoxetine hydrochloride
Navigation: NDC > Supplier starting with: P > PAR PHARMACEUTICAL, INC| Field | Value |
|---|---|
| NDC Code: | 49884-734 |
| Proprietary Name: | Fluoxetine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | fluoxetine hydrochloride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 13-01-2010 |
| Category Name: | ANDA |
| Application Number: | ANDA075755 |
| Labeler: | PAR PHARMACEUTICAL, INC |
| Substance Name: | FLUOXETINE HYDROCHLORIDE |
| Active Numerator Strength: | 10 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
| DEA Schedule: |