Rosuvastatin Calcium
- Product NDC
- 50090-5189
- 11-digit product format
- 500905189
- Labeler code
- 50090
- Product ID
- 50090-5189_68b52be2-fca7-4329-89f2-bac216c405a1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA206465
- Marketing category
- ANDA
- Marketing start
- 2017-03-21
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 83MVU38M7Q | ROSUVASTATIN CALCIUM | 147098-20-2 | ROSUVASTATIN CALCIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-5189-0 | 50090518900 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-5189-0) | 2020-09-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Rosuvastatin Calcium | A-S Medication Solutions | 2023-09-10 | Human Prescription Drug Label | 5 |