PRAVASTATIN SODIUM
- Product NDC
- 63629-8911
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209869
- Marketing category
- ANDA
- Substance
- PRAVASTATIN SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 63629-8911-1 | 1000 TABLET in 1 BOTTLE (63629-8911-1) | 20211119 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| dcf46d0c-87da-4009-b238-eb5cf287c3ed | These highlights do not include all the information needed to use PRAVASTATIN SODIUM TABLETS safely and effectively. See full prescribing information for PRAVASTATIN SODIUM TABLETS. PRAVASTATIN SODIUM tablets, for oral use Initial U.S. Approval: 1991 | Bryant Ranch Prepack | 2025-04-23 | HUMAN PRESCRIPTION DRUG LABEL | 103 |