Pravastatin Sodium
- Product NDC
- 43353-964
- 11-digit product format
- 433530964
- Labeler code
- 43353
- Product ID
- 43353-964_0d6fa0b8-bef8-42ff-8b4e-ea21b291a8e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA076056
- Marketing category
- ANDA
- Marketing start
- 2014-06-17
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43353-964 | PRAVASTATIN SODIUM (PRAVASTATIN SODIUM) TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 2 | Legacy NDC | 20210316_576f2e65-2bf6-4f6b-8538-50221f2d88bb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43353-964-45 | 43353096445 | 45 TABLET in 1 BOTTLE (43353-964-45) | 45 tablet | 2014-09-26 | 0000-00-00 | No | No | Current |