Finasteride - Finasteride
Navigation: NDC > Supplier starting with: N > NEW HORIZON RX GROUP, LLC| Field | Value |
|---|---|
| NDC Code: | 58517-200 |
| Proprietary Name: | Finasteride |
| Suffix: | |
| Non-Proprietary Name: | Finasteride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 13-08-2013 |
| Category Name: | ANDA |
| Application Number: | ANDA090121 |
| Labeler: | NEW HORIZON RX GROUP, LLC |
| 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: |