Rosuvastatin calcium
- Product NDC
- 70518-1169
- 11-digit product format
- 705181169
- Labeler code
- 70518
- Product ID
- 70518-1169_90872064-7f06-9450-e053-2a95a90aaf66
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA206434
- Marketing category
- ANDA
- Marketing start
- 2018-05-11
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record