Pravastatin Sodium
- Product NDC
- 63629-6758
- 11-digit product format
- 636296758
- Labeler code
- 63629
- Product ID
- 63629-6758_b56e7cc4-2e04-4747-8ce1-7826f4a37e56
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076056
- Marketing category
- ANDA
- Marketing start
- 2006-04-25
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6758-1 | 63629675801 | 30 TABLET in 1 BOTTLE (63629-6758-1) | 30 tablet | 2015-09-22 | 0000-00-00 | No | No | Current |