Venlafaxine Hydrochloride - Venlafaxine Hydrochloride
Navigation: NDC > Supplier starting with: A > AUROBINDO PHARMA LIMITED| Field | Value |
|---|---|
| NDC Code: | 65862-528 |
| Proprietary Name: | Venlafaxine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Venlafaxine Hydrochloride |
| Dosage Form: | CAPSULE, EXTENDED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 01-06-2011 |
| Category Name: | ANDA |
| Application Number: | ANDA200834 |
| Labeler: | AUROBINDO PHARMA LIMITED |
| Substance Name: | VENLAFAXINE HYDROCHLORIDE |
| Active Numerator Strength: | 75 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
| DEA Schedule: |