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Lescol
Lescol - 0078-0176-05 - (fluvastatin sodium)
Drug Information of Lescol
| Product NDC: | 0078-0176 |
| Proprietary Name: | Lescol |
| Non Proprietary Name: | fluvastatin sodium |
| Active Ingredient(s): | 20 mg/1 & nbsp; fluvastatin sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lescol
| Product NDC: | 0078-0176 |
| Labeler Name: | Novartis Pharmaceuticals Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020261 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19931230 |
Package Information of Lescol
| Package NDC: | 0078-0176-05 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (0078-0176-05) |
NDC Information of Lescol
| NDC Code | 0078-0176-05 |
| Proprietary Name | Lescol |
| Package Description | 100 CAPSULE in 1 BOTTLE (0078-0176-05) |
| Product NDC | 0078-0176 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluvastatin sodium |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19931230 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Pharmaceuticals Corporation |
| Substance Name | FLUVASTATIN SODIUM |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
