PRAVASTATIN SODIUM
- Product NDC
- 61919-707
- 11-digit product format
- 619190707
- Labeler code
- 61919
- Product ID
- 61919-707_94f32fcc-8ea9-6760-e053-2995a90a61fd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA207068
- Marketing category
- ANDA
- Marketing start
- 2018-12-19
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 10 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-707-30 | PRAVASTATIN SODIUM | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 61919-707-90 | PRAVASTATIN SODIUM | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-707 | PRAVASTATIN SODIUM TABLET [DIRECT RX] | 3 | Legacy NDC, 2 package rows | 20230706_7d660b83-99fa-6ef2-e053-2991aa0a9d97.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-707-30 | 61919070730 | 30 TABLET in 1 BOTTLE (61919-707-30) | 30 tablet | 2018-12-19 | 0000-00-00 | No | No | Current |
| 61919-707-90 | 61919070790 | 90 TABLET in 1 BOTTLE (61919-707-90) | 90 tablet | 2018-12-19 | 0000-00-00 | No | No | Current |