Pravastatin Sodium
- Product NDC
- 42254-202
- 11-digit product format
- 422540202
- Labeler code
- 42254
- Product ID
- 42254-202_3ff75342-03b6-462f-b6db-80bc1a52fe6c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA077987
- Marketing category
- ANDA
- Marketing start
- 2007-05-11
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 20 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pravastatin Sodium Tablets | Rebel Distributors Corp | 2012-04-11 | HUMAN PRESCRIPTION DRUG LABEL | 1 |