Atorvastatin Calcium
- Product NDC
- 68788-8132
- 11-digit product format
- 687888132
- Labeler code
- 68788
- Product ID
- 68788-8132_5d3c35d6-de7d-433e-a5e9-3831685ff4e6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA204991
- Marketing category
- ANDA
- Marketing start
- 2022-02-03
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM TRIHYDRATE
- Active strength
- 80 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 |
|---|
| 68788-8132-1 | 68788813201 | 100 TABLET in 1 BOTTLE (68788-8132-1) | 100 tablet | 2022-02-03 | 0000-00-00 | No | No | Current |
| 68788-8132-3 | 68788813203 | 30 TABLET in 1 BOTTLE (68788-8132-3) | 30 tablet | 2022-02-03 | 0000-00-00 | No | No | Current |
| 68788-8132-6 | 68788813206 | 60 TABLET in 1 BOTTLE (68788-8132-6) | 60 tablet | 2022-02-03 | 0000-00-00 | No | No | Current |
| 68788-8132-9 | 68788813209 | 90 TABLET in 1 BOTTLE (68788-8132-9) | 90 tablet | 2022-02-03 | 0000-00-00 | No | No | Current |