| NDC Code | 0093-7446-01 |
|---|
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7446-01) |
|---|
| Product NDC | 0093-7446 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Fluvastatin Sodium |
|---|
| Non-Proprietary Name | Fluvastatin Sodium |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20160602 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA079011 |
|---|
| Manufacturer | Teva Pharmaceuticals USA, Inc. |
|---|
| Substance Name | FLUVASTATIN SODIUM |
|---|
| Strength | 80 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
|---|