atorvastatin calcium
- Product NDC
- 70771-1444
- 11-digit product format
- 707711444
- Labeler code
- 70771
- Product ID
- 70771-1444_09caa07b-012e-4af9-9e91-02fbdfb929a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atorvastatin calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA206536
- Marketing category
- ANDA
- Marketing start
- 2018-11-21
- 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 |
|---|
| 70771-1444 | ATORVASTATIN CALCIUM TABLET [ZYDUS LIFESCIENCES LIMITED] | 6 | Legacy NDC | 20241023_cda119f2-54c8-4a08-b266-a0dbd214d2ce.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1444-0 | 70771144400 | 1000 TABLET in 1 BOTTLE (70771-1444-0) | 1000 tablet | 2018-11-21 | 0000-00-00 | No | No | Current |
| 70771-1444-1 | 70771144401 | 100 TABLET in 1 BOTTLE (70771-1444-1) | 100 tablet | 2018-11-21 | 0000-00-00 | No | No | Current |
| 70771-1444-3 | 70771144403 | 30 TABLET in 1 BOTTLE (70771-1444-3) | 30 tablet | 2018-11-21 | 0000-00-00 | No | No | Current |
| 70771-1444-4 | 70771144404 | 10 BLISTER PACK in 1 CARTON (70771-1444-4) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2018-11-21 | 0000-00-00 | No | No | Current |
| 70771-1444-5 | 70771144405 | 500 TABLET in 1 BOTTLE (70771-1444-5) | 500 tablet | 2018-11-21 | 0000-00-00 | No | No | Current |
| 70771-1444-9 | 70771144409 | 90 TABLET in 1 BOTTLE (70771-1444-9) | 90 tablet | 2018-11-21 | 0000-00-00 | No | No | Current |