Atomoxetine Hydrochloride - Atomoxetine Hydrochloride
Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL FZE| Field | Value |
|---|---|
| NDC Code: | 47335-817 |
| Proprietary Name: | Atomoxetine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Atomoxetine Hydrochloride |
| Dosage Form: | CAPSULE |
| Method: | ORAL |
| Original Marketing Date: | 05-10-2010 |
| Category Name: | ANDA |
| Application Number: | ANDA079020 |
| Labeler: | SUN PHARMA GLOBAL FZE |
| Substance Name: | ATOMOXETINE HYDROCHLORIDE |
| Active Numerator Strength: | 40 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA] |
| DEA Schedule: |