Lovastatin - Lovastatin
Navigation: NDC > Supplier starting with: A > AVKARE, INC.| Field | Value |
|---|---|
| NDC Code: | 42291-376 |
| Proprietary Name: | Lovastatin |
| Suffix: | |
| Non-Proprietary Name: | Lovastatin |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 06-06-2002 |
| Category Name: | ANDA |
| Application Number: | ANDA075991 |
| Labeler: | AVKARE, INC. |
| Substance Name: | LOVASTATIN |
| Active Numerator Strength: | 20 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
| DEA Schedule: |