Atorvastatin Calcium
- Product NDC
- 50090-5298
- 11-digit product format
- 500905298
- Labeler code
- 50090
- Product ID
- 50090-5298_87a92ec7-47e7-4599-80f5-09e0c8f523bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076477
- Marketing category
- ANDA
- Marketing start
- 2011-12-01
- 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 |
|---|
| 50090-5298-0 | Atorvastatin Calcium | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 3 |
| 50090-5298-1 | Atorvastatin Calcium | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5298 | ATORVASTATIN CALCIUM TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 2 package rows | 20210416_b378ec00-a711-4ca3-9d79-ae3328258179.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5298-0 | 50090529800 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-5298-0) | 2020-10-27 | 0000-00-00 | No | No | Current |
| 50090-5298-1 | 50090529801 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-5298-1) | 2020-10-27 | 0000-00-00 | No | No | Current |