Pravastatin Sodium
- Product NDC
- 50090-6898
- 11-digit product format
- 500906898
- Labeler code
- 50090
- Product ID
- 50090-6898_36e7610c-5f4a-49bd-a45e-492757aea7ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076056
- Marketing category
- ANDA
- Marketing start
- 2006-04-25
- 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 |
|---|
| 50090-6898-0 | 50090689800 | 90 TABLET in 1 BOTTLE (50090-6898-0) | 90 tablet | 2023-12-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pravastatin Sodium | A-S Medication Solutions | 2023-12-15 | HUMAN PRESCRIPTION DRUG LABEL | 1 |