Pravastatin sodium
- Product NDC
- 50090-2785
- 11-digit product format
- 500902785
- Labeler code
- 50090
- Product ID
- 50090-2785_75a7aeff-657f-45db-b532-901d6b41cb47
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076939
- Marketing category
- ANDA
- Marketing start
- 2007-12-28
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 80 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 50090-2785-0 | Pravastatin sodium | 30 in 1 BOTTLE | TABLET | 30 | | 9 |
| 50090-2785-1 | Pravastatin sodium | 90 in 1 BOTTLE | TABLET | 90 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2785 | PRAVASTATIN SODIUM TABLET [A-S MEDICATION SOLUTIONS] | 9 | Legacy NDC, 2 package rows | 20180518_11695064-d2f9-4bbf-9205-00e89da95b08.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2785-0 | 50090278500 | 30 in 1 BOTTLE | Historical |
| 50090-2785-1 | 50090278501 | 90 in 1 BOTTLE | Historical |