Pravastatin Sodium
- Product NDC
- 68071-3788
- 11-digit product format
- 680713788
- Labeler code
- 68071
- Product ID
- 68071-3788_2d40e472-0660-e50a-e063-6294a90abc30
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- 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 |
|---|
| 68071-3788-9 | 68071378809 | 90 TABLET in 1 BOTTLE (68071-3788-9) | 90 tablet | 2025-02-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pravastatin Sodium | NuCare Pharmaceuticals, Inc. | 2025-02-03 | HUMAN PRESCRIPTION DRUG LABEL | 1 |