PRAVASTATIN SODIUM
- Product NDC
- 61919-731
- 11-digit product format
- 619190731
- Labeler code
- 61919
- Product ID
- 61919-731_9caca164-0e32-7ed3-e053-2995a90a1244
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DirectRX
- Application
- ANDA076939
- Marketing category
- ANDA
- Marketing start
- 2015-12-28
- 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
- 2021-12-31
- 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 |
|---|
| 61919-731-90 | PRAVASTATIN SODIUM | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-731 | PRAVASTATIN SODIUM TABLET [DIRECTRX] | 2 | Legacy NDC, 1 package rows | 20200131_27fb491a-033e-60df-e054-00144ff88e88.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 |
|---|
| 61919-731-90 | 61919073190 | 90 TABLET in 1 BOTTLE (61919-731-90) | 90 tablet | 2015-12-28 | 0000-00-00 | No | No | Current |