Rosuvastatin calcium
- Product NDC
- 71335-1501
- 11-digit product format
- 713351501
- Labeler code
- 71335
- Product ID
- 71335-1501_a309752f-ed99-489e-b117-36adc6bfb224
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA079172
- Marketing category
- ANDA
- Marketing start
- 2016-07-19
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 71335-1501-1 | 71335150101 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1501-1) | 2020-02-18 | 0000-00-00 | No | No | Current |
| 71335-1501-2 | 71335150102 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1501-2) | 2020-02-18 | 0000-00-00 | No | No | Current |
| 71335-1501-3 | 71335150103 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-1501-3) | 2020-02-18 | 0000-00-00 | No | No | Current |
| 71335-1501-4 | 71335150104 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1501-4) | 2020-02-18 | 0000-00-00 | No | No | Current |