ATORVASTATIN CALCIUM
- Product NDC
- 68071-4396
- 11-digit product format
- 680714396
- Labeler code
- 68071
- Product ID
- 68071-4396_bb7c1f26-b120-0b83-e053-2a95a90aa0e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATORVASTATIN CALCIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA090548
- Marketing category
- ANDA
- Marketing start
- 2012-05-29
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM TRIHYDRATE
- Active strength
- 10 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 |
|---|
| 68071-4396-3 | ATORVASTATIN CALCIUM | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 3 |
| 68071-4396-6 | ATORVASTATIN CALCIUM | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-4396 | ATORVASTATIN CALCIUM TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.] | 3 | Legacy NDC, 2 package rows | 20210217_6a2275fd-30bf-7900-e053-2a91aa0a949a.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 |
|---|
| 68071-4396-3 | 68071439603 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-4396-3) | 2018-04-18 | 0000-00-00 | No | No | Current |
| 68071-4396-6 | 68071439606 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-4396-6) | 2018-04-18 | 0000-00-00 | No | No | Current |