Atorvastatin calcium
- Product NDC
- 70518-4474
- 11-digit product format
- 705184474
- Labeler code
- 70518
- Product ID
- 70518-4474_4d4eaa19-e8e2-e86c-e063-6294a90a1737
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA217081
- Marketing category
- ANDA
- Marketing start
- 2025-09-10
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Atorvastatin calcium
- Listing expiration
- 2027-12-31
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 |
|---|
| 70518-4474-0 | Atorvastatin calcium | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | | 2 |
| 70518-4474-1 | Atorvastatin calcium | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4474-0 | 70518447400 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4474-0) | 2025-09-10 | No | No | Historical |
| 70518-4474-1 | 70518447401 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4474-1) | 2026-03-18 | No | No | Historical |