ATORVASTATIN CALCIUM
- Product NDC
- 68788-7618
- 11-digit product format
- 687887618
- Labeler code
- 68788
- Product ID
- 68788-7618_dc593659-8a26-435a-8114-956e77d03fda
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATORVASTATIN CALCIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090548
- Marketing category
- ANDA
- Marketing start
- 2020-02-14
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE
- Active strength
- 10 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 |
|---|
| 68788-7618-1 | 68788761801 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7618-1) | 2020-02-14 | 0000-00-00 | No | No | Current |
| 68788-7618-3 | 68788761803 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7618-3) | 2020-02-14 | 0000-00-00 | No | No | Current |
| 68788-7618-6 | 68788761806 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7618-6) | 2020-02-14 | 0000-00-00 | No | No | Current |
| 68788-7618-9 | 68788761809 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7618-9) | 2020-02-14 | 0000-00-00 | No | No | Current |