Atorvastatin calcium
- Product NDC
- 68788-8298
- 11-digit product format
- 687888298
- Labeler code
- 68788
- Product ID
- 68788-8298_716ed987-055a-42bc-90ef-c62f78ed85f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA213853
- Marketing category
- ANDA
- Marketing start
- 2022-11-29
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN
- Active strength
- 40 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-8298 | ATORVASTATIN CALCIUM TABLET [PREFERRED PHARMACEUTICALS INC.] | 4 | Legacy NDC | 20250207_716ed987-055a-42bc-90ef-c62f78ed85f4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8298-1 | 68788829801 | 100 TABLET in 1 BOTTLE (68788-8298-1) | 100 tablet | 2022-11-29 | 0000-00-00 | No | No | Current |
| 68788-8298-3 | 68788829803 | 30 TABLET in 1 BOTTLE (68788-8298-3) | 30 tablet | 2022-11-29 | 0000-00-00 | No | No | Current |
| 68788-8298-6 | 68788829806 | 60 TABLET in 1 BOTTLE (68788-8298-6) | 60 tablet | 2022-11-29 | 0000-00-00 | No | No | Current |
| 68788-8298-9 | 68788829809 | 90 TABLET in 1 BOTTLE (68788-8298-9) | 90 tablet | 2022-11-29 | 0000-00-00 | No | No | Current |