NDC 48433-149-01 - Pravastatin sodium
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 48433-149
- Requested NDC
- 48433-149-01
- Package NDCs from labels
- 48433-149-01, 48433-149-20
- Manufacturer
- Safecor Health LLC
- Effective date
- 2026-07-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Pravastatin sodium - Safecor Health LLC | Safecor Health LLC | 2026-07-01 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| 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 Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 48433-149-20 | EA - Each | 48433-149 | 456b4cb6-6614-41ba-a22d-0e7e3a2d1b5f | 1 | 2026-05-22 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| MEDULLOSSEINUM PLEX | ARNICA MONTANA, CALCAREA PHOSPHORICA, CALENDULA OFFICINALIS, HYPERICUM PERFORATUM, MEDULLOSSEINUM, PULSATILLA, RUTA GRAVEOLENS, SYMPHYTUM OFFICINALE | Seroyal USA | 22b7eafe-ef76-0677-e054-00144ff88e88 | 2020-10-09 | Warnings | L11K75P92J |
| PRAVASTATIN SODIUM | PRAVASTATIN SODIUM | Proficient Rx LP | 63ca6179-6ae3-4f0b-bdca-50d200317921 | 2019-10-01 | Warnings, Adverse reactions | 904475 3M8608UQ61 |
| Pravastatin sodium | PRAVASTATIN SODIUM | Dr.Reddy's Laboratories Limited | 99cc0546-bb2d-751e-edfd-1c15a1182e0c | 2018-11-21 | Warnings, Adverse reactions | 904458 904467 904475 3M8608UQ61 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.