NDC 70518-3476-01 - 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
- 70518-3476
- Requested NDC
- 70518-3476-01
- Package NDCs from labels
- 70518-3476-0, 70518-3476-1, 70518-3476-2, 70518-3476-3, 70518-3476-4, 70518-3476-5, 70518-3476-6, 70518-3476-7, 70518-3476-8, 70518-3476-9, 70518-3476-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-07-30
- 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. | 2026-07-30 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-3476-0 | prednisone | 21 in 1 BLISTER PACK | TABLET | 21 | 18 | |
| 70518-3476-1 | prednisone | 30 in 1 BLISTER PACK | TABLET | 30 | 18 | |
| 70518-3476-2 | prednisone | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | 18 | |
| 70518-3476-3 | prednisone | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | 18 | |
| 70518-3476-4 | prednisone | 40 in 1 BOTTLE, PLASTIC | TABLET | 40 | 18 | |
| 70518-3476-5 | prednisone | 10 in 1 BOTTLE, PLASTIC | TABLET | 10 | 18 | |
| 70518-3476-6 | prednisone | 14 in 1 BOTTLE, PLASTIC | TABLET | 14 | 18 | |
| 70518-3476-7 | prednisone | 20 in 1 BOTTLE, PLASTIC | TABLET | 20 | 18 | |
| 70518-3476-8 | prednisone | 35 in 1 BOTTLE, PLASTIC | TABLET | 35 | 18 | |
| 70518-3476-9 | prednisone | 40 in 1 BOTTLE, PLASTIC | TABLET | 40 | 18 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-3476 | PREDNISONE TABLET [REMEDYREPACK INC.] | 11 | Current NDC, Legacy NDC, 10 package rows | 20241006_5218e88b-468b-4d60-ab7e-78cca632b23a.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 Tablets, USP, 20 mg | PREDNISONE | Bryant Ranch Prepack | 852ea185-1bda-4c89-a192-ee0f93cba428 | 2026-03-11 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| Prednisone | PREDNISONE | A-S Medication Solutions | 71295010-5adb-499b-a03a-5c78b5e79b2d | 2026-03-07 | Warnings, Adverse reactions | VB0R961HZT |
| prednisone | PREDNISONE | Asclemed USA, Inc. | fdcf3271-fae7-47ef-a370-adbdc0a3cf37 | 2026-03-03 | Warnings, Adverse reactions | ANDA208412 198145 312615 198148 VB0R961HZT |
| PREDNISONE | PREDNISONE | NuCare Pharmaceuticals, Inc. | 2760a808-b076-5887-e063-6294a90a79ae | 2026-02-27 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| PREDNISONE | PREDNISONE | QPharma, Inc. | 4aa286e3-e272-8095-e063-6394a90ae871 | 2026-02-13 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| PREDNISONE | PREDNISONE | ASCLEMED USA INC. | bf6ebe58-e7bb-49d3-842e-3372f8ba6172 | 2026-02-05 | Warnings, Adverse reactions | 198145 312615 198148 VB0R961HZT |
| PREDNISONE | PREDNISONE | NuCare Pharmaceuticals, Inc. | 292e2529-711c-7b74-e063-6394a90a660d | 2026-02-04 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| prednisone | PREDNISONE | Sportpharm LLC | 0e3d2f62-2b02-4ddf-a983-abb71ff31e36 | 2026-02-03 | Warnings, Adverse reactions | ANDA208412 198145 312615 VB0R961HZT |
| PREDNISONE | PREDNISONE | REMEDYREPACK INC. | ab9bffed-b1a2-4e82-ac45-bee40b41060f | 2026-02-02 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| Prednisone | PREDNISONE | Cardinal Health 107, LLC | 199ed6a6-d9d9-49de-b383-5933a026591b | 2026-01-27 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| Prednisone | PREDNISONE | A-S Medication Solutions | efe0c82b-9dd9-4729-b06f-06307867aca0 | 2026-01-20 | Warnings, Adverse reactions | 198145 312615 VB0R961HZT |
| Lotrimin Daily Sweat and Odor Control | TOPICAL STARCH | Bayer HealthCare LLC. | 9ec5c80d-b550-496f-e053-2a95a90a5489 | 2026-01-16 | Warnings | O8232NY3SJ |
| prednisone | PREDNISONE | Coupler LLC | 47bb25d2-f33c-96ce-e063-6394a90a069e | 2026-01-06 | Warnings, Adverse reactions | ANDA208412 VB0R961HZT |
| prednisone | PREDNISONE | Northwind Health Company, LLC | f2a15b5d-f540-2582-e053-2995a90a591a | 2026-01-01 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | Northwind Health Company, LLC | faf6c0c5-e5f4-4de5-e053-6294a90abd1a | 2026-01-01 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | Northwind Health Company, LLC | f6cb7924-4190-f130-e053-6294a90a21fe | 2026-01-01 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| prednisone | PREDNISONE | Northwind Health Company, LLC | f2f1a2ea-fa1b-b4f1-e053-2995a90aa276 | 2026-01-01 | Warnings, Adverse reactions | ANDA208412 198148 VB0R961HZT |
| PredniSONE | PREDNISONE | Northwind Health Company, LLC | ab315be2-8d13-be25-e053-2995a90a5184 | 2026-01-01 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | Northwind Health Company, LLC | 0f377d9f-b2f4-4dae-b503-5f963bea281f | 2026-01-01 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| PredniSONE | PREDNISONE | Northwind Health Company, LLC | dad4f191-8893-48e0-e053-2995a90ae864 | 2026-01-01 | Warnings, Adverse reactions | 198145 VB0R961HZT |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.