Pravastatin Sodium
- Product NDC
- 61919-708
- 11-digit product format
- 619190708
- Labeler code
- 61919
- Product ID
- 61919-708_0e994ad4-d03f-9670-e063-6294a90adad3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA207068
- Marketing category
- ANDA
- Marketing start
- 2019-01-15
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 40 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 |
|---|
| 61919-708-30 | 61919070830 | 30 TABLET in 1 BOTTLE (61919-708-30) | 30 tablet | 2019-01-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pravastatin Sodium | Direct_Rx | 2024-01-10 | HUMAN PRESCRIPTION DRUG LABEL | 3 |