Rosuvastatin Calcium
- Product NDC
- 55700-839
- 11-digit product format
- 557000839
- Labeler code
- 55700
- Product ID
- 55700-839_89efc9e7-e755-4530-bb7c-7e9993ce1962
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA079172
- Marketing category
- ANDA
- Marketing start
- 2020-01-24
- 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 |
|---|
| 55700-839-30 | 55700083930 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-839-30) | 2020-01-24 | 0000-00-00 | No | No | Current |