Rosuvastatin
- Product NDC
- 50090-2723
- 11-digit product format
- 500902723
- Labeler code
- 50090
- Product ID
- 50090-2723_4071a7a9-4cdb-496d-a17e-f29bfab5df1d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA207616
- Marketing category
- ANDA
- Marketing start
- 2016-10-29
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2723 | ROSUVASTATIN TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 25 | Legacy NDC | 20230317_d286336a-c602-4a45-90a6-ade1d7faf29d.zip |