Atorvastatin calcium
- Product NDC
- 70518-3304
- 11-digit product format
- 705183304
- Labeler code
- 70518
- Product ID
- 70518-3304_4ef25c36-8b48-d731-e063-6394a90acf42
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin calcium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA211933
- Marketing category
- ANDA
- Marketing start
- 2021-12-22
- 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
- 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 | 80 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 48A5M73Z4Q |
| Rxcui | 259255 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-3304-0 | Atorvastatin calcium | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 8 |
| 70518-3304-1 | Atorvastatin calcium | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 8 |
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 |
|---|
| 70518-3304-0 | 70518330400 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3304-0) | 2021-12-22 | 0000-00-00 | No | No | Current |
| 70518-3304-1 | 70518330401 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3304-1) | 2022-12-06 | | No | No | Historical |