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Fluvastatin Sodium
Fluvastatin Sodium - 0378-8020-77 - (fluvastatin)
Drug Information of Fluvastatin Sodium
| Product NDC: | 0378-8020 |
| Proprietary Name: | Fluvastatin Sodium |
| 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 Sodium
| Product NDC: | 0378-8020 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090595 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130319 |
Package Information of Fluvastatin Sodium
| Package NDC: | 0378-8020-77 |
| Package Description: | 90 CAPSULE in 1 BOTTLE, PLASTIC (0378-8020-77) |
NDC Information of Fluvastatin Sodium
| NDC Code | 0378-8020-77 |
| Proprietary Name | Fluvastatin Sodium |
| Package Description | 90 CAPSULE in 1 BOTTLE, PLASTIC (0378-8020-77) |
| Product NDC | 0378-8020 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluvastatin |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130319 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | FLUVASTATIN SODIUM |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
