Rosuvastatin Calcium
- Product NDC
- 70518-2774
- 11-digit product format
- 705182774
- Labeler code
- 70518
- Product ID
- 70518-2774_d70c1885-7357-3ff1-e053-2a95a90ae9ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rosuvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA208898
- Marketing category
- ANDA
- Marketing start
- 2020-06-09
- 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
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 |
|---|
| 70518-2774-0 | 70518277400 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2774-0) | 2020-06-09 | 0000-00-00 | No | No | Current |
| 70518-2774-1 | 70518277401 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2774-1) | 2021-01-19 | 0000-00-00 | No | No | Current |