Fluoxetine Hydrochloride - Fluoxetine Hydrochloride
Navigation: NDC > Supplier starting with: S > SANDOZ INC| Field | Value |
|---|---|
| NDC Code: | 0781-2822 |
| Proprietary Name: | Fluoxetine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Fluoxetine Hydrochloride |
| Dosage Form: | CAPSULE |
| Method: | ORAL |
| Original Marketing Date: | 29-01-2002 |
| Category Name: | ANDA |
| Application Number: | ANDA075049 |
| Labeler: | SANDOZ INC |
| Substance Name: | FLUOXETINE HYDROCHLORIDE |
| Active Numerator Strength: | 20 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
| DEA Schedule: |