Sertraline Hydrochloride - Sertraline Hydrochloride
Navigation: NDC > Supplier starting with: A > AUROLIFE PHARMA LLC| Field | Value |
|---|---|
| NDC Code: | 13107-012 |
| Proprietary Name: | Sertraline Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Sertraline Hydrochloride |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 15-03-2011 |
| Category Name: | ANDA |
| Application Number: | ANDA077206 |
| Labeler: | AUROLIFE PHARMA LLC |
| Substance Name: | SERTRALINE HYDROCHLORIDE |
| Active Numerator Strength: | 50 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
| DEA Schedule: |