Rosuvastatin Calcium
- Product NDC
- 50090-7005
- 11-digit product format
- 500907005
- Labeler code
- 50090
- Product ID
- 50090-7005_1dd8e099-9ec4-429b-8235-407443dccbb8
- 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
- 2019-06-27
- 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
- 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 |
|---|
| 50090-7005-0 | 50090700500 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7005-0) | 2024-01-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Rosuvastatin Calcium | A-S Medication Solutions | 2024-01-07 | HUMAN PRESCRIPTION DRUG LABEL | 4 |