Atorvastatin calcium
- Product NDC
- 69539-096
- 11-digit product format
- 695390096
- Labeler code
- 69539
- Product ID
- 69539-096_4bb92478-91aa-4be6-8e3a-4162b22dea25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- MSN LABORATORIES PRIVATE LIMITED
- Application
- ANDA211933
- Marketing category
- ANDA
- Marketing start
- 2019-02-08
- 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
- 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 |
|---|
| 69539-096 | ATORVASTATIN CALCIUM TABLET, FILM COATED [MSN LABORATORIES PRIVATE LIMITED] | 12 | Legacy NDC | 20240614_99eba422-e3d9-4e49-b4b4-3be6af258baa.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69539-096-05 | 69539009605 | 500 TABLET, FILM COATED in 1 BOTTLE (69539-096-05) | 2019-02-08 | 0000-00-00 | No | No | Current |
| 69539-096-30 | 69539009630 | 30 TABLET, FILM COATED in 1 BOTTLE (69539-096-30) | 2019-02-08 | 0000-00-00 | No | No | Current |
| 69539-096-90 | 69539009690 | 90 TABLET, FILM COATED in 1 BOTTLE (69539-096-90) | 2019-02-08 | 0000-00-00 | No | No | Current |
| 69539-096-99 | 69539009699 | 1000 TABLET, FILM COATED in 1 BOTTLE (69539-096-99) | 2021-05-10 | 0000-00-00 | No | No | Current |