Pravastatin sodium
- Product NDC
- 71335-2848
- 11-digit product format
- 713352848
- Labeler code
- 71335
- Product ID
- 71335-2848_34873359-fe19-4061-9912-c35509f9f9ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209869
- Marketing category
- ANDA
- Marketing start
- 2021-02-01
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 10 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 |
|---|
| 3M8608UQ61 | PRAVASTATIN SODIUM | 81131-70-6 | PRAVASTATIN SODIUM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2848-1 | 71335284801 | 90 TABLET in 1 BOTTLE (71335-2848-1) | 90 tablet | 2025-11-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pravastatin sodium | Bryant Ranch Prepack | 2025-11-10 | HUMAN PRESCRIPTION DRUG LABEL | 100 |