Rosuvastatin Calcium
- Product NDC
- 42292-029
- 11-digit product format
- 422920029
- Labeler code
- 42292
- Product ID
- 42292-029_7d8ee399-0c5f-a796-e053-2a91aa0a607f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- rosuvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA079161
- Marketing category
- ANDA
- Marketing start
- 2016-08-15
- Marketing end
- 2019-05-31
- Substance
- ROSUVASTATIN CALCIUM
- Active strength
- 5 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