Rosuvastatin Calcium
- Product NDC
- 70934-245
- 11-digit product format
- 709340245
- Labeler code
- 70934
- Product ID
- 70934-245_a71f78ba-c32d-fdca-e053-2995a90a7e3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA208898
- Marketing category
- ANDA
- Marketing start
- 2019-01-22
- 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
- 2021-12-31
- 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 |
|---|
| 70934-245-30 | 70934024530 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-245-30) | 2019-01-22 | 0000-00-00 | No | No | Current |
| 70934-245-90 | 70934024590 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-245-90) | 2019-05-15 | 0000-00-00 | No | No | Current |
| 70934-245-96 | 70934024596 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-245-96) | 2020-05-28 | 0000-00-00 | No | No | Current |