PRAVASTATIN SODIUM
- Product NDC
- 68071-5001
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076341
- Marketing category
- ANDA
- Substance
- PRAVASTATIN SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-5001-3 | 30 TABLET in 1 BOTTLE (68071-5001-3) | 2019-07-26 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| PRAVASTATIN SODIUM | NuCare Pharmaceuticals,Inc. | 2024-06-18 | HUMAN PRESCRIPTION DRUG LABEL | 3 |