Atorvastatin Calcium
- Product NDC
- 71335-2225
- 11-digit product format
- 713352225
- Labeler code
- 71335
- Product ID
- 71335-2225_98a82149-92c6-4667-94e4-63487201823a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin Calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA214659
- Marketing category
- ANDA
- Marketing start
- 2022-08-29
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 48A5M73Z4Q | ATORVASTATIN CALCIUM TRIHYDRATE | 344423-98-9 | ATORVASTATIN CALCIUM TRIHYDRATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2225-1 | 71335222501 | 30 TABLET in 1 BOTTLE (71335-2225-1) | 30 tablet | 2023-10-09 | No | No | Historical |
| 71335-2225-2 | 71335222502 | 60 TABLET in 1 BOTTLE (71335-2225-2) | 60 tablet | 2024-07-16 | No | No | Historical |
| 71335-2225-3 | 71335222503 | 90 TABLET in 1 BOTTLE (71335-2225-3) | 90 tablet | 2023-09-29 | No | No | Historical |
| 71335-2225-4 | 71335222504 | 180 TABLET in 1 BOTTLE (71335-2225-4) | 180 tablet | 2024-07-16 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Atorvastatin Calcium | Bryant Ranch Prepack | 2024-07-16 | HUMAN PRESCRIPTION DRUG LABEL | 101 |