Atorvastatin calcium
- Product NDC
- 70518-4321
- 11-digit product format
- 705184321
- Labeler code
- 70518
- Product ID
- 70518-4321_402e6f6e-bc5c-cd8c-e063-6294a90a7196
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA213853
- Marketing category
- ANDA
- Marketing start
- 2025-03-27
- Substance
- ATORVASTATIN
- 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 | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | A0JWA85V8F |
| Rxcui | 617311 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4321-0 | Atorvastatin calcium | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-4321 | ATORVASTATIN CALCIUM TABLET [REMEDYREPACK INC.] | 1 | Current NDC, 1 package rows | 20250331_604a011e-6c64-4895-8f6e-d28f119c4c22.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4321-0 | 70518432100 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-4321-0) | 100 tablet | 2025-03-27 | No | No | Historical |