Rosuvastatin
- Product NDC
- 68071-2326
- 11-digit product format
- 680712326
- Labeler code
- 68071
- Product ID
- 68071-2326_b8522357-23de-d834-e053-2995a90a2a58
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA207616
- Marketing category
- ANDA
- Marketing start
- 2016-10-29
- Marketing end
- 0000-00-00
- Substance
- ROSUVASTATIN CALCIUM
- Active strength
- 10 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68071-2326-9 | Rosuvastatin | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2326 | ROSUVASTATIN TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC, 1 package rows | 20210108_b85227e5-1838-7591-e053-2a95a90ace49.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2326-9 | 68071232609 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-2326-9) | 2021-01-07 | 0000-00-00 | No | No | Current |