Pravastatin sodium
- Product NDC
- 57237-165
- 11-digit product format
- 572370165
- Labeler code
- 57237
- Product ID
- 57237-165_e5ef567c-556d-4df2-a369-b0e7cd1058b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rising Health, LLC
- Application
- ANDA203367
- Marketing category
- ANDA
- Marketing start
- 2017-02-02
- 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
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57237-165-05 | 57237016505 | 500 TABLET in 1 BOTTLE (57237-165-05) | 500 tablet | 2017-02-02 | 0000-00-00 | No | No | Current |
| 57237-165-90 | 57237016590 | 90 TABLET in 1 BOTTLE (57237-165-90) | 90 tablet | 2017-02-02 | 0000-00-00 | No | No | Current |
| 57237-165-99 | 57237016599 | 1000 TABLET in 1 BOTTLE (57237-165-99) | 1000 tablet | 2017-02-02 | 0000-00-00 | No | No | Current |