ATORVASTATIN CALCIUM
- Product NDC
- 68071-2468
- 11-digit product format
- 680712468
- Labeler code
- 68071
- Product ID
- 68071-2468_c67b6c7b-455b-2315-e053-2a95a90a0cee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATORVASTATIN CALCIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA207687
- Marketing category
- ANDA
- Marketing start
- 2018-08-06
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM TRIHYDRATE
- Active strength
- 40 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2468 | ATORVASTATIN CALCIUM TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC | 20210707_c67b5d5d-6bf0-d0ad-e053-2995a90a9cc9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2468-3 | 68071246803 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-2468-3) | 2021-07-06 | 0000-00-00 | No | No | Current |
| 68071-2468-6 | 68071246806 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-2468-6) | 2021-07-06 | 0000-00-00 | No | No | Current |