Rosuvastatin Calcium
- Product NDC
- 49884-262
- 11-digit product format
- 498840262
- Labeler code
- 49884
- Product ID
- 49884-262_b4a8bf61-cdfd-4775-aa23-8bca571bc6a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- rosuvastatin calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA079168
- Marketing category
- ANDA
- Marketing start
- 2016-07-19
- Marketing end
- 2020-08-31
- Substance
- ROSUVASTATIN CALCIUM
- Active strength
- 20 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