Pravastatin sodium
- Product NDC
- 48433-149
- 11-digit product format
- 484330149
- Labeler code
- 48433
- Product ID
- 48433-149_49ef1f35-49ba-be39-e063-6394a90a9c8d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Safecor Health LLC
- Application
- ANDA076056
- Marketing category
- ANDA
- Marketing start
- 2026-01-28
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 40 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pravastatin sodium
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PRAVASTATIN SODIUM | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3M8608UQ61 |
| Rxcui | 904467, 904475 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48433-149-01 | Pravastatin sodium | 1 in 1 BLISTER PACK | TABLET | 1 | | 4 |
| 48433-149-20 | Pravastatin sodium | 100 in 1 CARTON | TABLET | 100 | | 4 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48433-149-01 | 48433014901 | 1 in 1 BLISTER PACK | | | | | Historical |
| 48433-149-20 | 48433014920 | 100 BLISTER PACK in 1 CARTON (48433-149-20) / 1 TABLET in 1 BLISTER PACK (48433-149-01) | 100 blister pack | 2026-01-28 | No | No | Historical |