Rosuvastatin Calcium
- Product NDC
- 70934-275
- 11-digit product format
- 709340275
- Labeler code
- 70934
- Product ID
- 70934-275_b557ee00-296a-1e4d-e053-2995a90a85b5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA206434
- Marketing category
- ANDA
- Marketing start
- 2019-02-14
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-275-30 | 70934027530 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-275-30) | 2020-06-10 | 0000-00-00 | No | No | Current |
| 70934-275-90 | 70934027590 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-275-90) | 2020-10-05 | 0000-00-00 | No | No | Current |
| 70934-275-96 | 70934027596 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-275-96) | 2019-02-14 | 0000-00-00 | No | No | Current |