Rosuvastatin Calcium
- Product NDC
- 71205-399
- 11-digit product format
- 712050399
- Labeler code
- 71205
- Product ID
- 71205-399_fe440b64-b5a5-4cc2-ae7c-ae313c145890
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA208898
- Marketing category
- ANDA
- Marketing start
- 2017-11-22
- Marketing end
- 2022-01-31
- Substance
- ROSUVASTATIN CALCIUM
- Active strength
- 5 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-399-30 | 71205039930 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-399-30) | 2020-02-07 | 2022-01-31 | No | No | Current |
| 71205-399-60 | 71205039960 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-399-60) | 2020-02-07 | 2022-01-31 | No | No | Current |
| 71205-399-90 | 71205039990 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-399-90) | 2020-02-07 | 2022-01-31 | No | No | Current |