atorvastatin calcium
- Product NDC
- 50090-4685
- 11-digit product format
- 500904685
- Labeler code
- 50090
- Product ID
- 50090-4685_6dc3b477-52b1-4d56-81a0-8d3e311d7b5b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atorvastatin calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA206536
- Marketing category
- ANDA
- Marketing start
- 2018-11-21
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-4685-0 | atorvastatin calcium | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 50090-4685-1 | atorvastatin calcium | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4685 | ATORVASTATIN CALCIUM TABLET [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 2 package rows | 20210416_46eb0d41-4c5a-496c-9084-d0dbd7883b62.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4685-0 | 50090468500 | 30 TABLET in 1 BOTTLE (50090-4685-0) | 30 tablet | 2019-11-05 | 0000-00-00 | No | No | Current |
| 50090-4685-1 | 50090468501 | 90 TABLET in 1 BOTTLE (50090-4685-1) | 90 tablet | 2019-11-05 | 0000-00-00 | No | No | Current |