NDC 50090-3137-04 - 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
- 50090-3137
- Requested NDC
- 50090-3137-04
- Package NDCs from labels
- 50090-3137-0, 50090-3137-5, 50090-3137-7, 50090-3137-1, 50090-3137-4, 50090-3137-8, 50090-3137-2, 50090-3137-04
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2025-07-03
- 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 | 2025-07-03 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50090-3137-0 | Prednisone | 10 in 1 BOTTLE | TABLET | 10 | 22 | |
| 50090-3137-1 | Prednisone | 15 in 1 BOTTLE | TABLET | 15 | 22 | |
| 50090-3137-2 | Prednisone | 21 in 1 BOTTLE | TABLET | 21 | 22 | |
| 50090-3137-4 | Prednisone | 50 in 1 BOTTLE | TABLET | 50 | 22 | |
| 50090-3137-5 | Prednisone | 30 in 1 BOTTLE | TABLET | 30 | 22 | |
| 50090-3137-7 | Prednisone | 100 in 1 BOTTLE | TABLET | 100 | 22 | |
| 50090-3137-8 | Prednisone | 40 in 1 BOTTLE | TABLET | 40 | 22 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50090-3137 | PREDNISONE (PREDNISONE) TABLET [A-S MEDICATION SOLUTIONS] | 19 | Current NDC, Legacy NDC, 7 package rows | 20240604_dc94273f-af06-4bd5-9ce3-ce0a0f36587b.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-3137-0 | EA - Each | 50090-3137 | a657058d-4baa-4a19-ad30-6768b205f924 | 1 | 2021-09-07 |
| 50090-3137-1 | EA - Each | 50090-3137 | 459ced8f-278f-46f1-8c35-b92884b0e58e | 1 | 2021-09-07 |
| 50090-3137-2 | EA - Each | 50090-3137 | 913b705b-8c71-4689-9a3c-9a71f15fb547 | 1 | 2019-05-02 |
| 50090-3137-4 | EA - Each | 50090-3137 | e77fd3e8-71fd-4201-978e-bc112def77eb | 1 | 2021-09-07 |
| 50090-3137-5 | EA - Each | 50090-3137 | 7b190702-04fe-496f-9858-078a269db30e | 1 | 2021-03-02 |
| 50090-3137-7 | EA - Each | 50090-3137 | 76d641e3-2e58-4ea6-ad47-fec5b3b3c530 | 1 | 2021-09-07 |
| 50090-3137-8 | EA - Each | 50090-3137 | 0525e86b-f560-4afe-a4f1-bfbde4b4702d | 1 | 2023-08-08 |
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 | Bryant Ranch Prepack | 290a91e5-22ae-4d62-ab34-39a3117002e2 | 2026-09-08 | Warnings, Adverse reactions | VB0R961HZT |
| prednisone | PREDNISONE | REMEDYREPACK INC. | 4750028a-30ad-420a-8e6b-06dc2429d433 | 2026-09-08 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| Prednisone | PREDNISONE | Bryant Ranch Prepack | 0062fcc7-aa08-4990-9d33-d798725907f1 | 2026-09-08 | Warnings, Adverse reactions | VB0R961HZT |
| PredniSONE | PREDNISONE | REMEDYREPACK INC. | 7db793b4-5768-4e9a-a47b-1ebbfed74001 | 2026-09-03 | Warnings, Adverse reactions | VB0R961HZT |
| PREDNISONE | PREDNISONE | REMEDYREPACK INC. | 0993b354-d936-472b-bafc-114f0f81bfb0 | 2026-09-01 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| PredniSONE | PREDNISONE | REMEDYREPACK INC. | 94715919-70bd-46c9-95fc-e151adf39cf9 | 2026-08-31 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| BMNP ALUMINUM OXIDE | ALUMINUM OXIDE | Total Operations Management LLC DBA:Bestmade Natural Products Micro | 5a5ad83a-0ecb-21fa-e063-6294a90a1422 | 2026-08-31 | Warnings | LMI26O6933 |
| prednisone | PREDNISONE | REMEDYREPACK INC. | 23b12d22-97d6-426e-bf9c-dd6c2ff77370 | 2026-08-26 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| PredniSONE Tablets, USP, 20 mg | PREDNISONE | PD-Rx Pharmaceuticals, Inc. | 6b360c1f-c862-47ee-a40e-3903c2d6162f | 2026-08-21 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| PredniSONE | PREDNISONE | Preferred Pharmaceuticals Inc. | 02158832-550b-4855-a5c5-6abbf13ed6f0 | 2026-08-20 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| Prednisone | PREDNISONE | Bryant Ranch Prepack | c60a07f9-ed9f-4434-a69d-2e2fea4843fd | 2026-08-20 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | REMEDYREPACK INC. | 746b0bcd-122e-4ea8-a824-28415073a38e | 2026-08-20 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | Bryant Ranch Prepack | 7ea7f6a9-78ef-42fe-baac-f817da3976fb | 2026-08-20 | Warnings, Adverse reactions | VB0R961HZT |
| prednisone | PREDNISONE | Preferred Pharmaceuticals Inc. | 1e74ac55-4a48-4bf5-bfed-36c0fa37dd9f | 2026-08-19 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| prednisone | PREDNISONE | Preferred Pharmaceuticals Inc. | fa75f5ce-8a74-4873-811f-7d9d9beec08f | 2026-08-19 | Warnings, Adverse reactions | VB0R961HZT |
| prednisone | PREDNISONE | Preferred Pharmaceuticals Inc. | 930b5eea-3ec8-47df-a76d-1e0bc0b5c5b2 | 2026-08-19 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | Preferred Pharmaceuticals, Inc. | f89bd1dc-88cd-4aef-a7ae-6310f38a3423 | 2026-08-19 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | Major Pharmaceuticals | 57b98930-92ab-4b77-a033-ae9895ee718a | 2026-08-19 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| prednisone | PREDNISONE | Preferred Pharmaceuticals Inc. | ce7663a7-4c91-4790-aa43-96f259b3bb18 | 2026-08-19 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| prednisone | PREDNISONE | REMEDYREPACK INC. | e47a0448-331f-4846-8e63-c52c3afa274b | 2026-08-11 | Warnings, Adverse reactions | 312615 VB0R961HZT |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.