Fluvastatin Sodium
- Product NDC
- 68151-1326
- 11-digit product format
- 681511326
- Labeler code
- 68151
- Product ID
- 68151-1326_3a755dcc-08e8-4965-8290-d3d4187d50f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluvastatin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA090595
- Marketing category
- ANDA
- Marketing start
- 2013-03-19
- Marketing end
- 0000-00-00
- Substance
- FLUVASTATIN SODIUM
- Active strength
- 20 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-1326-9 | Fluvastatin Sodium | 1 in 1 PACKAGE | CAPSULE | 1 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-1326 | FLUVASTATIN SODIUM (FLUVASTATIN) CAPSULE [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20140707_e2dddb57-aea3-45f2-ad06-2b209a8d934b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-1326-9 | 68151132609 | 1 in 1 PACKAGE | Historical |