Rosuvastatin Calcium
- Product NDC
- 70518-2090
- 11-digit product format
- 705182090
- Labeler code
- 70518
- Product ID
- 70518-2090_dad06ea5-30bc-e49e-e053-2a95a90a7997
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA208898
- Marketing category
- ANDA
- Marketing start
- 2019-05-21
- Marketing end
- 0000-00-00
- Substance
- ROSUVASTATIN CALCIUM
- Active strength
- 40 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2090-2 | 70518209002 | 45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2090-2) | 2020-10-08 | 0000-00-00 | No | No | Current |