Atorvastatin Calcium
- Product NDC
- 42708-144
- 11-digit product format
- 427080144
- Labeler code
- 42708
- Product ID
- 42708-144_4586b1ba-5c21-e661-e063-6294a90a59be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- QPharma, Inc.
- Application
- ANDA209288
- Marketing category
- ANDA
- Marketing start
- 2018-12-23
- Substance
- ATORVASTATIN CALCIUM TRIHYDRATE
- Active strength
- 40 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Atorvastatin Calcium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ATORVASTATIN CALCIUM TRIHYDRATE | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 48A5M73Z4Q |
| Rxcui | 617311 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42708-144-30 | Atorvastatin Calcium | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42708-144 | ATORVASTATIN CALCIUM TABLET, FILM COATED [QPHARMA, INC.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250523_c0e2a5d0-1aa3-e131-e053-2a95a90a9870.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 |
|---|
| 42708-144-30 | 42708014430 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-144-30) | 2021-04-23 | 0000-00-00 | Yes | No | Current |