Rosuvastatin calcium
- Product NDC
- 50090-5056
- 11-digit product format
- 500905056
- Labeler code
- 50090
- Product ID
- 50090-5056_aebb5121-21a7-4217-985f-a91316b7b3fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA079172
- Marketing category
- ANDA
- Marketing start
- 2016-07-19
- Marketing end
- 0000-00-00
- Substance
- ROSUVASTATIN CALCIUM
- Active strength
- 10 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 50090-5056-0 | 50090505600 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-5056-0) | 2020-05-22 | 0000-00-00 | No | No | Current |