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Fluvastatin
Fluvastatin - 0093-7442-56 - (Fluvastatin)
Drug Information of Fluvastatin
| Product NDC: | 0093-7442 |
| Proprietary Name: | Fluvastatin |
| Non Proprietary Name: | Fluvastatin |
| Active Ingredient(s): | 20 mg/1 & nbsp; Fluvastatin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluvastatin
| Product NDC: | 0093-7442 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078407 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120705 |
Package Information of Fluvastatin
| Package NDC: | 0093-7442-56 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (0093-7442-56) |
NDC Information of Fluvastatin
| NDC Code | 0093-7442-56 |
| Proprietary Name | Fluvastatin |
| Package Description | 30 CAPSULE in 1 BOTTLE (0093-7442-56) |
| Product NDC | 0093-7442 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluvastatin |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120705 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | FLUVASTATIN SODIUM |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
