PRAVASTATIN SODIUM
- Product NDC
- 50090-7709
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077987
- Marketing category
- ANDA
- Substance
- PRAVASTATIN SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7709-0 | 30 TABLET in 1 BOTTLE (50090-7709-0) | 2025-10-14 | | No | Historical |
| 50090-7709-1 | 90 TABLET in 1 BOTTLE (50090-7709-1) | 2025-10-14 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| PRAVASTATIN SODIUM | A-S Medication Solutions | 2025-10-15 | HUMAN PRESCRIPTION DRUG LABEL | 1 |