PRAVASTATIN SODIUM
- Product NDC
- 61919-801
- 11-digit product format
- 619190801
- Labeler code
- 61919
- Product ID
- 61919-801_ea4ec601-5971-1928-e053-2995a90adc38
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA077751
- Marketing category
- ANDA
- Marketing start
- 2019-10-04
- 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
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-801-90 | 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 |
|---|
| 61919-801 | PRAVASTATIN SODIUM TABLET [DIRECT_RX] | 3 | Legacy NDC, 1 package rows | 20240111_7f814fd9-7b35-67da-e053-2a91aa0a39dc.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 |
|---|
| 61919-801-30 | 61919080130 | 30 TABLET in 1 BOTTLE (61919-801-30) | 30 tablet | 2019-10-05 | 0000-00-00 | No | No | Current |
| 61919-801-90 | 61919080190 | 90 TABLET in 1 BOTTLE (61919-801-90) | 90 tablet | 2019-03-29 | 0000-00-00 | No | No | Current |