Rosuvastatin calcium
- Product NDC
- 68071-4765
- 11-digit product format
- 680714765
- Labeler code
- 68071
- Product ID
- 68071-4765_bb8dadce-a0d8-bc7b-e053-2995a90a9b3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA206434
- Marketing category
- ANDA
- Marketing start
- 2016-10-31
- Marketing end
- 0000-00-00
- Substance
- ROSUVASTATIN CALCIUM
- Active strength
- 5 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 |
|---|
| 68071-4765-9 | 68071476509 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-4765-9) | 2019-02-13 | 0000-00-00 | No | No | Current |