Azelastine Hydrochloride - Azelastine Hydrochloride
Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL FZE| Field | Value |
|---|---|
| NDC Code: | 47335-938 |
| Proprietary Name: | Azelastine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Azelastine Hydrochloride |
| Dosage Form: | SOLUTION/ DROPS |
| Method: | INTRAOCULAR |
| Original Marketing Date: | 31-05-2010 |
| Category Name: | ANDA |
| Application Number: | ANDA078738 |
| Labeler: | SUN PHARMA GLOBAL FZE |
| Substance Name: | AZELASTINE HYDROCHLORIDE |
| Active Numerator Strength: | .5 |
| Active Ingredient Unit: | mg/mL |
| Pharm Classes: | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC] |
| DEA Schedule: |