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 | PREDNISONE | Aurobindo Pharma Limited | b1ac4c92-e1fd-4015-b172-0932790ae019 | 2024-02-16 | Warnings, Adverse reactions | 198145 312615 198148 VB0R961HZT |
| Prednisone | PREDNISONE | NuCare Pharmaceuticals,Inc. | 63102d75-9b2b-84a9-e053-2a91aa0a317d | 2024-02-09 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | A-S Medication Solutions | 410988ea-456a-454e-932c-fcbdbef04ba9 | 2024-01-18 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| Prednisone | PREDNISONE | A-S Medication Solutions | 44069d49-4cf4-4f1e-9fbd-b496c6ca81a1 | 2024-01-18 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| prednisone | PREDNISONE | A-S Medication Solutions | 17278e0a-cbff-4a95-96ee-f34f7466faa0 | 2023-11-24 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | Chartwell RX, LLC | 92483276-d55c-42c6-8bbc-27137ff25296 | 2023-09-06 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| prednisone | PREDNISONE | Proficient Rx LP | 6a0c1192-8ce4-466d-a0f3-d878d67349cf | 2023-09-01 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| Prednisone | PREDNISONE | Proficient Rx LP | 5961b1d4-6a4c-452f-b3f1-c99f3a9a6445 | 2023-09-01 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| PredniSONE | PREDNISONE | A-S Medication Solutions | 0060b86b-0b79-4c54-a7be-97683a933a05 | 2023-08-31 | Warnings, Adverse reactions | VB0R961HZT |
| PredniSONE | PREDNISONE | A-S Medication Solutions | f11c190e-edf8-454d-82c4-1ed769b5a6d2 | 2023-08-31 | Warnings, Adverse reactions | VB0R961HZT |
| PredniSONE | PREDNISONE | A-S Medication Solutions | 6f0719a2-1759-4354-9363-bb9fb3bddb3d | 2023-08-31 | Warnings, Adverse reactions | VB0R961HZT |
| prednisone | PREDNISONE | Proficient Rx LP | 6ec5b58c-65e9-47ee-b2ac-7d0b395a0630 | 2023-07-01 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| prednisone | PREDNISONE | Proficient Rx LP | 22d9fd96-cad5-4762-9a56-0ff63357ed9e | 2023-02-01 | Warnings, Adverse reactions | ANDA208412 198148 VB0R961HZT |
| prednisone | PREDNISONE | NCS HealthCare of KY, LLC dba Vangard Labs | bc37cc2e-2f6a-4131-bb6a-63b6e576df21 | 2022-11-11 | Warnings, Adverse reactions | VB0R961HZT |
| prednisone | PREDNISONE | NCS HealthCare of KY, LLC dba Vangard Labs | 202f6840-f3bd-4bed-ab5d-b36d3c4cdf0f | 2022-11-10 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | PharmPak, Inc. | 03aaf69f-d9c7-433c-baea-9c6eca0fe1e5 | 2022-10-08 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| Prednisone | PREDNISONE | Proficient Rx LP | 71d70ec6-859a-4951-af98-248a864e1135 | 2022-09-01 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| PredniSONE | PREDNISONE | Proficient Rx LP | e109f428-ca85-4a2c-acd0-ca8d498e7723 | 2022-06-01 | Warnings, Adverse reactions | 198148 VB0R961HZT |
| Prednisone | PREDNISONE | Proficient Rx LP | 67681e4e-3002-4428-af5e-6ff1a950b037 | 2022-05-02 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| Prednisone | PREDNISONE | Proficient Rx LP | a1bff575-cd79-4596-99f1-30a5fe8a8b4c | 2022-05-01 | Warnings, Adverse reactions | VB0R961HZT |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.