PRAVASTATIN SODIUM
- Product NDC
- 63629-8909
- 11-digit product format
- 636298909
- Labeler code
- 63629
- Product ID
- 63629-8909_3366c587-a3d3-cc3f-e063-6394a90a9c37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209869
- Marketing category
- ANDA
- Marketing start
- 2021-02-01
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PRAVASTATIN SODIUM
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PRAVASTATIN SODIUM | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3M8608UQ61 |
| Rxcui | 904467 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-8909-1 | PRAVASTATIN SODIUM | 1000 in 1 BOTTLE | TABLET | 1000 | | 105 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-8909 | PRAVASTATIN SODIUM TABLET [BRYANT RANCH PREPACK] | 105 | Current NDC, Legacy NDC, 1 package rows | 20250424_0bb2f1e8-9405-4f06-9a33-5ba06765a8e7.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 |
|---|
| 63629-8909-1 | 63629890901 | 1000 TABLET in 1 BOTTLE (63629-8909-1) | 1000 tablet | 2021-11-19 | 0000-00-00 | No | No | Current |