Rosuvastatin calcium
- Product NDC
- 63629-8124
- 11-digit product format
- 636298124
- Labeler code
- 63629
- Product ID
- 63629-8124_381bd14e-09b4-44d1-8ae6-7875a2fc80c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206434
- Marketing category
- ANDA
- Marketing start
- 2016-10-31
- 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
- 2023-12-31
- 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 |
|---|
| 63629-8124-1 | 63629812401 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8124-1) | 2019-07-15 | 0000-00-00 | No | No | Current |
| 63629-8124-2 | 63629812402 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-8124-2) | 2022-01-18 | 0000-00-00 | No | No | Current |