Rosuvastatin calcium
- Product NDC
- 50090-3177
- 11-digit product format
- 500903177
- Labeler code
- 50090
- Product ID
- 50090-3177_42c4f64b-ed36-4a10-8d1a-1df12f70e557
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA206434
- Marketing category
- ANDA
- Marketing start
- 2016-10-31
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3177-0 | 50090317700 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-3177-0) | 2017-10-16 | 0000-00-00 | No | No | Current |
| 50090-3177-1 | 50090317701 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3177-1) | 2016-10-31 | 0000-00-00 | No | No | Current |