Pravastatin sodium
- Product NDC
- 68071-3895
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA076056
- Marketing category
- ANDA
- Substance
- PRAVASTATIN SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3895-9 | 90 TABLET in 1 BOTTLE (68071-3895-9) | 2025-09-16 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pravastatin sodium | NuCare Pharmaceuticals, Inc. | 2025-10-27 | HUMAN PRESCRIPTION DRUG LABEL | 2 |
| Pravastatin sodium | NuCare Pharmaceuticals, Inc. | 2025-09-16 | HUMAN PRESCRIPTION DRUG LABEL | 1 |