Atorvastatin Calcium
- Product NDC
- 68788-7979
- 11-digit product format
- 687887979
- Labeler code
- 68788
- Product ID
- 68788-7979_fe413945-a6ab-49ec-94ec-534e670b35f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA204991
- Marketing category
- ANDA
- Marketing start
- 2021-07-28
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM TRIHYDRATE
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7979-1 | 68788797901 | 100 TABLET in 1 BOTTLE (68788-7979-1) | 100 tablet | 2021-07-28 | 0000-00-00 | No | No | Current |
| 68788-7979-3 | 68788797903 | 30 TABLET in 1 BOTTLE (68788-7979-3) | 30 tablet | 2021-07-28 | 0000-00-00 | No | No | Current |
| 68788-7979-6 | 68788797906 | 60 TABLET in 1 BOTTLE (68788-7979-6) | 60 tablet | 2021-07-28 | 0000-00-00 | No | No | Current |
| 68788-7979-9 | 68788797909 | 90 TABLET in 1 BOTTLE (68788-7979-9) | 90 tablet | 2021-07-28 | 0000-00-00 | No | No | Current |