PRAVASTATIN SODIUM
- Product NDC
- 61919-709
- 11-digit product format
- 619190709
- Labeler code
- 61919
- Product ID
- 61919-709_7ab587c5-5f5c-079e-e053-2991aa0a6d81
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA207068
- Marketing category
- ANDA
- Marketing start
- 2018-11-15
- 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
- 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 |
|---|
| 61919-709-90 | PRAVASTATIN SODIUM | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-709 | PRAVASTATIN SODIUM TABLET [DIRECT RX] | 1 | Legacy NDC, 1 package rows | 20190211_7ab587c5-5f5b-079e-e053-2991aa0a6d81.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 |
|---|
| 61919-709-90 | 61919070990 | 90 TABLET in 1 BOTTLE (61919-709-90) | 90 tablet | 2018-11-15 | 0000-00-00 | No | No | Current |