Rosuvastatin Calcium
- Product NDC
- 0093-7573
- 11-digit product format
- 000937573
- Labeler code
- 0093
- Product ID
- 0093-7573_83cfa277-158e-466a-8fcf-703495f858f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA079166
- Marketing category
- ANDA
- Marketing start
- 2016-08-18
- Marketing end
- 2019-10-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record