Atorvastatin calcium
- Product NDC
- 82804-056
- 11-digit product format
- 828040056
- Labeler code
- 82804
- Product ID
- 82804-056_acbbd2c4-60bd-4e01-ad7a-b9b3178569f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atorvastatin calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA213853
- Marketing category
- ANDA
- Marketing start
- 2020-08-26
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| A0JWA85V8F | ATORVASTATIN | 134523-00-5 | ATORVASTATIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-056-30 | 82804005630 | 30 TABLET in 1 BOTTLE (82804-056-30) | 30 tablet | 2024-01-12 | No | No | Historical |
| 82804-056-60 | 82804005660 | 60 TABLET in 1 BOTTLE (82804-056-60) | 60 tablet | 2024-01-12 | No | No | Historical |
| 82804-056-90 | 82804005690 | 90 TABLET in 1 BOTTLE (82804-056-90) | 90 tablet | 2024-01-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Atorvastatin calcium | Proficient Rx LP | 2024-01-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |