ATORVASTATIN CALCIUM
- Product NDC
- 51407-079
- 11-digit product format
- 514070079
- Labeler code
- 51407
- Product ID
- 51407-079_dd824969-e57c-631d-e053-2995a90ae173
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATORVASTATIN CALCIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA205519
- Marketing category
- ANDA
- Marketing start
- 2016-05-19
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM TRIHYDRATE
- Active strength
- 20 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 |
|---|
| 51407-079 | ATORVASTATIN CALCIUM TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.] | 12 | Legacy NDC | 20241027_75a0d6b3-7a5d-3458-e053-2a91aa0a702e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-079-05 | 51407007905 | 500 TABLET, FILM COATED in 1 BOTTLE (51407-079-05) | 2018-09-12 | 0000-00-00 | No | No | Current |
| 51407-079-90 | 51407007990 | 90 TABLET, FILM COATED in 1 BOTTLE (51407-079-90) | 2018-09-12 | 0000-00-00 | No | No | Current |