NDC 68788-8166-01 - 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
- 68788-8166
- Requested NDC
- 68788-8166-01
- Package NDCs from labels
- 68788-8166-2, 68788-8166-3, 68788-8166-1, 68788-8166-6, 68788-8166-8, 68788-8166-4, 68788-8166-7, 68788-8166-5, 68788-8166-9, 68788-8166-01
- Manufacturer
- Preferred Pharmaceuticals Inc.
- Effective date
- 2026-08-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PredniSONE Tablets USP Rx only | Preferred Pharmaceuticals Inc. | 2026-08-19 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68788-8166-1 | prednisone | 10 in 1 BOTTLE | TABLET | 10 | 4 | |
| 68788-8166-2 | prednisone | 21 in 1 BOTTLE | TABLET | 21 | 4 | |
| 68788-8166-3 | prednisone | 30 in 1 BOTTLE | TABLET | 30 | 4 | |
| 68788-8166-4 | prednisone | 40 in 1 BOTTLE | TABLET | 40 | 4 | |
| 68788-8166-5 | prednisone | 50 in 1 BOTTLE | TABLET | 50 | 4 | |
| 68788-8166-6 | prednisone | 15 in 1 BOTTLE | TABLET | 15 | 4 | |
| 68788-8166-7 | prednisone | 45 in 1 BOTTLE | TABLET | 45 | 4 | |
| 68788-8166-8 | prednisone | 20 in 1 BOTTLE | TABLET | 20 | 4 | |
| 68788-8166-9 | prednisone | 90 in 1 BOTTLE | TABLET | 90 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68788-8166 | PREDNISONE TABLET [PREFERRED PHARMACEUTICALS INC.] | 3 | Current NDC, Legacy NDC, 9 package rows | 20240802_ce7663a7-4c91-4790-aa43-96f259b3bb18.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68788-8166-2 | EA - Each | 68788-8166 | 2020bcf0-d766-4da1-a20b-e38f0202ad64 | 1 | 2022-05-04 |
| 68788-8166-3 | EA - Each | 68788-8166 | 9b366ff2-474b-4909-b444-fbdf7562d2ce | 1 | 2022-05-04 |
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 | Sportpharm LLC | 5dde7256-d3b8-400d-a0eb-c60078bfc5d9 | 2026-04-24 | Warnings, Adverse reactions | ANDA208412 198148 VB0R961HZT |
| Caldesene Baby | STARCH, CORN AND ZINC OXIDE | Insight Pharmaceuticals LLC | 9f12dee2-7afa-45e9-a729-0fd42bb77715 | 2026-04-22 | Warnings | O8232NY3SJ |
| Caldesene Medicated Protecting | CORNSTARCH AND ZINC OXIDE | Insight Pharmaceuticals LLC | ffc92a0f-a7cf-4a46-b2f1-089df2bbb96b | 2026-04-22 | Warnings | O8232NY3SJ |
| prednisone | PREDNISONE | Amneal Pharmaceuticals NY LLC | 0740ef68-7641-432e-bd46-4710687fc9d7 | 2026-04-14 | Warnings, Adverse reactions | VB0R961HZT |
| Prednisone | PREDNISONE | REMEDYREPACK INC. | 4bd86b2f-75cb-4711-85e2-b81ed947cb13 | 2026-04-13 | Warnings, Adverse reactions | VB0R961HZT |
| prednisone | PREDNISONE | REMEDYREPACK INC. | e9a74862-6a3b-4247-837a-389761b5c352 | 2026-04-13 | Warnings, Adverse reactions | ANDA208412 VB0R961HZT |
| prednisone | PREDNISONE | REMEDYREPACK INC. | b540f4af-8f07-4c56-b151-d759440c514a | 2026-04-13 | Warnings, Adverse reactions | ANDA208412 198148 VB0R961HZT |
| Prednisone D/P | PREDNISONE D/P | Direct_Rx | 4f0a3946-025c-798a-e063-6294a90a831b | 2026-04-09 | Warnings, Adverse reactions | VB0R961HZT |
| prednisone | PREDNISONE | Bryant Ranch Prepack | 70d05ed7-5c4e-4cd1-84cd-0dbe90692c54 | 2026-04-09 | Warnings, Adverse reactions | ANDA208412 198148 VB0R961HZT |
| Prednisone | PREDNISONE | Northwind Health Company, LLC | fbd3f0c3-06b3-c9b4-e053-6294a90a6fdd | 2026-04-07 | Warnings, Adverse reactions | 198148 VB0R961HZT |
| PredniSONE Tablets, USP, 5 mg | PREDNISONE | PD-Rx Pharmaceuticals, Inc. | 251e9fe7-b1f5-4b5b-b5fa-8c8be43e284e | 2026-03-27 | Warnings, Adverse reactions | VB0R961HZT |
| PredniSONE Tablets, USP, 20 mg | PREDNISONE | PD-Rx Pharmaceuticals, Inc. | 3befbdc5-7d20-41b6-ad80-98e1c6b8caf5 | 2026-03-27 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| PREDNISONE | PREDNISONE | A-S Medication Solutions | 53c66f70-58fd-4d4c-b054-e5cefdc0c637 | 2026-03-26 | Warnings, Adverse reactions | VB0R961HZT |
| PredniSONE Tablets, USP, 5 mg | PREDNISONE | PD-Rx Pharmaceuticals, Inc. | d6df3295-3118-49af-be05-b1fab0d4adaa | 2026-03-25 | Warnings, Adverse reactions | VB0R961HZT |
| PredniSONE Tablets, USP, 10 mg | PREDNISONE | PD-Rx Pharmaceuticals, Inc. | 14d50f54-410b-45b2-a639-31498ceaf854 | 2026-03-25 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| Prednisone | PREDNISONE | A-S Medication Solutions | b5b088b9-8f90-468f-b7a4-a5274aa0aec9 | 2026-03-19 | Warnings, Adverse reactions | 198145 312615 VB0R961HZT |
| Prednisone D/P | PREDNISONE D/P | Direct_Rx | 41ade439-59f2-dfd1-e063-6294a90aca0f | 2026-03-17 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| PREDNISONE | PREDNISONE | DIRECT RX | 2a053775-6f6a-455e-b9a8-8b60e6062db3 | 2026-03-17 | Warnings, Adverse reactions | VB0R961HZT |
| PREDNISONE | PREDNISONE | A-S Medication Solutions | e753e2bc-acca-46eb-888c-ae72fcac6ca4 | 2026-03-13 | Warnings, Adverse reactions | VB0R961HZT |
| PREDNISONE | PREDNISONE | A-S Medication Solutions | a8f6298a-1084-4226-bfd9-a543a26ad2e7 | 2026-03-13 | Warnings, Adverse reactions | VB0R961HZT |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.