ATORVASTATIN CALCIUM
- Product NDC
- 68071-3714
- 11-digit product format
- 680713714
- Labeler code
- 68071
- Product ID
- 68071-3714_373efe2d-f2c0-ad83-e063-6294a90accef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATORVASTATIN CALCIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA214344
- Marketing category
- ANDA
- Marketing start
- 2023-09-12
- Substance
- ATORVASTATIN CALCIUM TRIHYDRATE
- Active strength
- 20 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3714-3 | 68071371403 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3714-3) | 2024-10-28 | No | No | Historical |
| 68071-3714-6 | 68071371406 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-3714-6) | 2024-11-20 | No | No | Historical |
| 68071-3714-9 | 68071371409 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3714-9) | 2025-01-31 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| ATORVASTATIN CALCIUM | NuCare Pharmaceuticals, Inc. | 2025-06-10 | HUMAN PRESCRIPTION DRUG LABEL | 4 |