NDC 70518-3539-01 - prednisone
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
- 70518-3539
- Requested NDC
- 70518-3539-01
- Package NDCs from labels
- 70518-3539-0, 70518-3539-1, 70518-3539-2, 70518-3539-3, 70518-3539-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-10-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PredniSONE Tablets USP Rx only | REMEDYREPACK INC. | 2026-10-13 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-3539-0 | prednisone | 30 in 1 BLISTER PACK | TABLET | 30 | 11 | |
| 70518-3539-1 | prednisone | 30 in 1 BLISTER PACK | TABLET | 30 | 11 | |
| 70518-3539-2 | prednisone | 180 in 1 BOTTLE, PLASTIC | TABLET | 180 | 11 | |
| 70518-3539-3 | prednisone | 21 in 1 BOTTLE, PLASTIC | TABLET | 21 | 11 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-3539 | PREDNISONE TABLET [REMEDYREPACK INC.] | 7 | Current NDC, Legacy NDC, 4 package rows | 20250507_e9a74862-6a3b-4247-837a-389761b5c352.zip |
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 |
|---|---|---|---|---|---|---|
| Prednisone | PREDNISONE | Proficient Rx LP | 35f504c3-1cf5-455d-8226-9ffeea606623 | 2022-05-01 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | Proficient Rx LP | 016d65c3-fff2-4e0c-9025-e2083cfa6a1f | 2022-04-01 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | Proficient Rx LP | 7d52bf53-76e3-4826-a12b-b16a8560bafc | 2021-05-01 | Warnings, Adverse reactions | 312617 VB0R961HZT |
| Prednisone | PREDNISONE | Asclemed USA, Inc. | dc663fd3-b149-48ae-a3f3-6abaa4808cc6 | 2020-08-28 | Warnings, Adverse reactions | 312617 VB0R961HZT |
| Prednisone | PREDNISONE | Proficient Rx LP | e4555299-af68-416f-8999-9bb703a45e77 | 2019-10-01 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | Proficient Rx LP | 7c650dc8-43f6-4257-81ed-c93b00202d06 | 2019-10-01 | Warnings, Adverse reactions | 312617 VB0R961HZT |
| Prednisone | PREDNISONE | Proficient Rx LP | 7a92b171-52ca-4948-81fc-e9a30597c5d8 | 2019-10-01 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | Aphena Pharma Solutions - Tennessee, LLC | b902ed21-c776-4046-8fbc-9ce95b16b139 | 2017-12-21 | Warnings, Adverse reactions | 312617 VB0R961HZT |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.