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 | PD-Rx Pharmaceuticals, Inc. | 15230866-f547-47bf-ac7d-19afd6a41e2e | 2026-06-04 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| PredniSONE Tablets, USP, 10 mg | PREDNISONE | PD-Rx Pharmaceuticals, Inc. | bb32e309-e3c7-4009-bcd4-d97545b7e975 | 2026-06-04 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| Prednisone | PREDNISONE | A-S Medication Solutions | aaaa3460-0239-4203-857f-0ada303c2108 | 2026-06-01 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| prednisone | PREDNISONE | Bryant Ranch Prepack | ecc48869-3812-4440-a398-749b28062059 | 2026-05-29 | Warnings, Adverse reactions | ANDA208412 198145 VB0R961HZT |
| prednisone | PREDNISONE | Bryant Ranch Prepack | 07d5e455-ac3b-4890-9619-609dd0be9106 | 2026-05-29 | Warnings, Adverse reactions | VB0R961HZT |
| prednisone | PREDNISONE | American Health Packaging | fdcd49a6-6cb1-49f8-9f4c-feb475c129b3 | 2026-05-21 | Warnings, Adverse reactions | ANDA208412 VB0R961HZT |
| prednisone | PREDNISONE | Cardinal Health 107, LLC | 1d797f3e-a46c-42bc-91bb-c570ae8ca8c2 | 2026-05-20 | Warnings, Adverse reactions | ANDA208412 VB0R961HZT |
| prednisone | PREDNISONE | REMEDYREPACK INC. | ea4070e1-080d-4feb-9561-3910c6b712dd | 2026-05-15 | Warnings, Adverse reactions | ANDA208412 198145 VB0R961HZT |
| PREDNISONE | PREDNISONE | ST. MARY'S MEDICAL PARK PHARMACY | 42e0decc-4d11-e7e6-e063-6394a90a9fcc | 2026-05-14 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| prednisone | PREDNISONE | REMEDYREPACK INC. | b3b70d6f-dc44-4a54-b39b-2762f37d5575 | 2026-05-13 | Warnings, Adverse reactions | ANDA208412 198145 VB0R961HZT |
| prednisone | PREDNISONE | QPharma Inc | 11870c93-fe64-e6c9-e063-6394a90a5334 | 2026-05-11 | Warnings, Adverse reactions | ANDA208412 VB0R961HZT |
| prednisone | PREDNISONE | QPharma Inc | f795ea1d-f41a-6100-e053-6394a90a63a4 | 2026-05-11 | Warnings, Adverse reactions | ANDA208412 198145 VB0R961HZT |
| Prednisone | PREDNISONE | A-S Medication Solutions | a6811c1f-3dad-46bb-b541-fddd2ff8e569 | 2026-05-08 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| Prednisone | PREDNISONE | Direct_Rx | f6051257-2144-4487-e053-2995a90a973b | 2026-05-05 | Warnings, Adverse reactions | ANDA208412 312615 VB0R961HZT |
| prednisone | PREDNISONE | Bryant Ranch Prepack | fbfd4e2b-3c8f-43c8-bcbe-da1ac4be75c5 | 2026-05-04 | Warnings, Adverse reactions | ANDA208412 312615 VB0R961HZT |
| Prednisone | PREDNISONE | Aphena Pharma Solutions - Tennessee, LLC | 18818282-68aa-82e9-e063-6394a90aef54 | 2026-05-01 | Warnings, Adverse reactions | VB0R961HZT |
| prednisone | PREDNISONE | Proficient Rx LP | 4b37ada5-1f22-46d5-a794-fd1477c0eb9b | 2026-05-01 | Warnings, Adverse reactions | ANDA208412 312615 VB0R961HZT |
| Prednisone delayed release | PREDNISONE | Dr. Reddys Laboratories Inc. | 474974ac-9811-c9f5-4050-58e535351d00 | 2026-04-30 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | Bryant Ranch Prepack | e4c1c8c5-0aa1-4531-aa7a-8567ac8dcba8 | 2026-04-29 | Warnings, Adverse reactions | VB0R961HZT |
| PREDNISONE | PREDNISONE | Coupler LLC | 50734a48-807d-cc00-e063-6294a90a4dae | 2026-04-27 | Warnings, Adverse reactions | 198148 VB0R961HZT |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.