ATORVASTATIN CALCIUM
- Product NDC
- 71205-731
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATORVASTATIN CALCIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA207687
- Marketing category
- ANDA
- Substance
- ATORVASTATIN CALCIUM TRIHYDRATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-731-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-731-30) | 2022-12-19 | | No | Historical |
| 71205-731-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-731-60) | 2022-12-19 | | No | Historical |
| 71205-731-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-731-90) | 2022-12-19 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| ATORVASTATIN CALCIUM | Proficient Rx LP | 2022-12-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |