PRAVASTATIN SODIUM
- Product NDC
- 71335-2908
- 11-digit product format
- 713352908
- Labeler code
- 71335
- Product ID
- 71335-2908_3e0f38e6-a515-4d76-9de4-34a83c38e8f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076341
- Marketing category
- ANDA
- Marketing start
- 2011-07-18
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 20 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 |
|---|
| 71335-2908-1 | 71335290801 | 1000 TABLET in 1 BOTTLE (71335-2908-1) | 1000 tablet | 2025-10-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| PRAVASTATIN SODIUM | Bryant Ranch Prepack | 2025-10-30 | HUMAN PRESCRIPTION DRUG LABEL | 100 |