Atorvastatin calcium
- Product NDC
- 68788-7563
- 11-digit product format
- 687887563
- Labeler code
- 68788
- Product ID
- 68788-7563_bf6a9b80-0d16-4271-b082-bbb8b9201519
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA211933
- Marketing category
- ANDA
- Marketing start
- 2019-02-08
- 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
- 2022-12-31
- 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 |
|---|
| 68788-7563-1 | 68788756301 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7563-1) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7563-3 | 68788756303 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7563-3) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7563-6 | 68788756306 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7563-6) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7563-9 | 68788756309 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7563-9) | 2019-12-27 | 0000-00-00 | No | No | Current |