Rosuvastatin calcium
- Product NDC
- 71205-008
- 11-digit product format
- 712050008
- Labeler code
- 71205
- Product ID
- 71205-008_d0887230-770f-41c5-8887-83ec83afc378
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA206434
- Marketing category
- ANDA
- Marketing start
- 2016-10-31
- 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 |
|---|
| 71205-008-30 | 71205000830 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-008-30) | 2018-04-02 | No | No | Historical |
| 71205-008-60 | 71205000860 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-008-60) | 2018-04-02 | No | No | Historical |
| 71205-008-90 | 71205000890 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-008-90) | 2018-04-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Rosuvastatin calcium | Proficient Rx LP | 2022-11-01 | HUMAN PRESCRIPTION DRUG LABEL | 5 |