Alfuzosin Hydrochloride - Alfuzosin Hydrochloride
Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL FZE| Field | Value |
|---|---|
| NDC Code: | 47335-956 |
| Proprietary Name: | Alfuzosin Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Alfuzosin Hydrochloride |
| Dosage Form: | TABLET, EXTENDED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 22-11-2011 |
| Category Name: | ANDA |
| Application Number: | ANDA079057 |
| Labeler: | SUN PHARMA GLOBAL FZE |
| Substance Name: | ALFUZOSIN HYDROCHLORIDE |
| Active Numerator Strength: | 10 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
| DEA Schedule: |