Atorvastatin Calcium
- Product NDC
- 70518-0567
- 11-digit product format
- 705180567
- Labeler code
- 70518
- Product ID
- 70518-0567_85d491f8-8b05-4d7a-e053-2991aa0a86a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atorvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091226
- Marketing category
- ANDA
- Marketing start
- 2017-06-06
- 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
- 2020-12-31
- 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 |
|---|
| 70518-0567 | ATORVASTATIN CALCIUM TABLET, FILM COATED [REMEDYREPACK INC.] | 10 | Legacy NDC | 20250429_cf07bd0f-7af7-4624-8d17-c3deb58ccfea.zip |