NDC 50090-7218-01 - 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
- 50090-7218
- Requested NDC
- 50090-7218-01
- Package NDCs from labels
- 50090-7218-2, 50090-7218-7, 50090-7218-4, 50090-7218-0, 50090-7218-8, 50090-7218-1, 50090-7218-5, 50090-7218-01
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2024-08-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| prednisone - A-S Medication Solutions | A-S Medication Solutions | 2024-08-15 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50090-7218-0 | prednisone | 10 in 1 BOTTLE | TABLET | 10 | 4 | |
| 50090-7218-1 | prednisone | 15 in 1 BOTTLE | TABLET | 15 | 4 | |
| 50090-7218-2 | prednisone | 21 in 1 BOTTLE | TABLET | 21 | 4 | |
| 50090-7218-4 | prednisone | 50 in 1 BOTTLE | TABLET | 50 | 4 | |
| 50090-7218-5 | prednisone | 30 in 1 BOTTLE | TABLET | 30 | 4 | |
| 50090-7218-7 | prednisone | 100 in 1 BOTTLE | TABLET | 100 | 4 | |
| 50090-7218-8 | prednisone | 40 in 1 BOTTLE | TABLET | 40 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50090-7218 | PREDNISONE TABLET [A-S MEDICATION SOLUTIONS] | 4 | Current NDC, 7 package rows | 20240816_f4cc64f8-781f-437a-a4a7-2d163026d1c2.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-7218-0 | EA - Each | 50090-7218 | d21d8a34-ea56-49df-8853-9a27486de3a1 | 1 | 2024-09-09 |
| 50090-7218-1 | EA - Each | 50090-7218 | 18c44860-9137-4a4c-a503-dc9c9565fa23 | 1 | 2024-09-09 |
| 50090-7218-2 | EA - Each | 50090-7218 | 7b0f0e4f-0fb6-47f4-80b7-e831d9759d63 | 1 | 2024-09-09 |
| 50090-7218-4 | EA - Each | 50090-7218 | 0e2f0f72-e4ae-4115-9c2c-c533bf72f570 | 1 | 2024-09-09 |
| 50090-7218-5 | EA - Each | 50090-7218 | 95b3eb57-0724-4848-a688-7e245fa6e5d4 | 1 | 2024-09-09 |
| 50090-7218-7 | EA - Each | 50090-7218 | bcb77984-f393-48f2-9b4c-0a5b746a317f | 1 | 2024-09-09 |
| 50090-7218-8 | EA - Each | 50090-7218 | 3bd95125-7037-4083-b85a-4724ca7c7e0a | 1 | 2024-09-09 |
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 | A-S Medication Solutions | 6f326242-786c-44b5-9317-f5fb0485d8e2 | 2025-10-12 | Warnings, Adverse reactions | VB0R961HZT |
| PredniSONE Tablets, USP, 10 mg | PREDNISONE | Bryant Ranch Prepack | 95b7de4c-9c69-45f6-9221-a2c87c441b04 | 2025-10-03 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| PredniSONE Tablets, USP, 5 mg | PREDNISONE | Bryant Ranch Prepack | 419058f7-7f30-41a1-964b-8eaa69290dea | 2025-10-03 | Warnings, Adverse reactions | VB0R961HZT |
| PredniSONE Tablets, USP, 20 mg | PREDNISONE | Bryant Ranch Prepack | b42adc18-21cc-4fe0-bf7d-fb76f4cda215 | 2025-10-03 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| PredniSONE Tablets, USP, 20 mg | PREDNISONE | Bryant Ranch Prepack | bfcc98b8-184e-4db4-8079-de88958c774b | 2025-09-26 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| PredniSONE Tablets, USP, 10 mg | PREDNISONE | Bryant Ranch Prepack | aba52f0c-0706-46ac-957d-e53963d35499 | 2025-09-26 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| prednisone | PREDNISONE | Coupler LLC | 3e0e3e28-e6ff-7b48-e063-6294a90a9acd | 2025-09-05 | Warnings, Adverse reactions | ANDA208412 198145 VB0R961HZT |
| PredniSONE Tablets, USP, 5 mg | PREDNISONE | Granulation Technology, Inc. | a173fcbb-99be-4b3e-a3a4-4e9ae04ad83f | 2025-08-15 | Warnings, Adverse reactions | 198145 312615 VB0R961HZT |
| PREDNISONE | PREDNISONE | Preferred Pharmaceuticals Inc. | 28130e6d-7cda-459a-9f80-cacaa82d71d3 | 2025-08-01 | Warnings, Adverse reactions | 198148 VB0R961HZT |
| Prednisone | PREDNISONE | A-S Medication Solutions | 74102cc5-7a1a-4a0f-a07f-a4b0f86bcabf | 2025-07-23 | Warnings, Adverse reactions | VB0R961HZT |
| PredniSONE | PREDNISONE | PD-Rx Pharmaceuticals, Inc. | f4500eb6-d24a-4247-83f4-99e73346e328 | 2025-07-17 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | A-S Medication Solutions | dc94273f-af06-4bd5-9ce3-ce0a0f36587b | 2025-07-03 | Warnings, Adverse reactions | 198145 312615 VB0R961HZT |
| PREDNISONE | PREDNISONE | NuCare Pharmaceuticals,Inc. | 27d8dcad-a024-ed85-e063-6394a90a420d | 2025-06-20 | Warnings, Adverse reactions | VB0R961HZT |
| PredniSONE Tablets, USP, 10 mg | PREDNISONE | Bryant Ranch Prepack | 136b98cd-60aa-4dc3-966c-488f4b7d6117 | 2025-05-05 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| PredniSONE Tablets, USP, 20 mg | PREDNISONE | Bryant Ranch Prepack | 48ee895b-dc3a-4f1f-8688-e06c217f449b | 2025-05-05 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| Prednisone | PREDNISONE | Proficient Rx LP | 08973b30-8576-4d31-aeef-934b72124e1f | 2025-05-01 | Warnings, Adverse reactions | VB0R961HZT |
| PREDNISONE | PREDNISONE | Preferred Pharmaceuticals Inc. | 60bb6698-d1fc-4720-9954-266a3d650f0d | 2025-04-29 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | Bryant Ranch Prepack | 0b2c2085-c4da-4441-ae5e-eefe26fd199e | 2025-04-25 | Warnings, Adverse reactions | VB0R961HZT |
| PredniSONE | PREDNISONE | Hikma Pharmaceuticals USA Inc. | 263ed4fa-3c29-4abb-9cb1-bc016bd34a05 | 2025-04-22 | Warnings, Adverse reactions | 198145 312615 VB0R961HZT |
| PredniSONE | PREDNISONE | Hikma Pharmaceuticals USA Inc. | 3115aef0-fd50-4ec8-a064-3effb695f3f2 | 2025-04-22 | Warnings, Adverse reactions | 198145 312615 198148 VB0R961HZT |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.