Atorvastatin Calcium
- Product NDC
- 68788-7900
- 11-digit product format
- 687887900
- Labeler code
- 68788
- Product ID
- 68788-7900_75445b2c-6a22-46d2-81fd-e89f2544aab8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA209288
- Marketing category
- ANDA
- Marketing start
- 2021-05-14
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-7900 | ATORVASTATIN CALCIUM TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.] | 5 | Legacy NDC | 20250206_7fc504dd-718a-4340-825f-e19ed76b71ef.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7900-1 | 68788790001 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7900-1) | 2021-05-14 | 0000-00-00 | No | No | Current |
| 68788-7900-3 | 68788790003 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7900-3) | 2021-05-14 | 0000-00-00 | No | No | Current |
| 68788-7900-6 | 68788790006 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7900-6) | 2021-05-14 | 0000-00-00 | No | No | Current |
| 68788-7900-9 | 68788790009 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7900-9) | 2021-05-14 | 0000-00-00 | No | No | Current |