FINASTERIDE - FINASTERIDE
Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL FZE| Field | Value |
|---|---|
| NDC Code: | 47335-715 |
| Proprietary Name: | FINASTERIDE |
| Suffix: | |
| Non-Proprietary Name: | FINASTERIDE |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 18-08-2011 |
| Category Name: | ANDA |
| Application Number: | ANDA090507 |
| Labeler: | SUN PHARMA GLOBAL FZE |
| Substance Name: | FINASTERIDE |
| Active Numerator Strength: | 5 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA] |
| DEA Schedule: |