NDC 67296-0140-04 - 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
- 67296-0140
- Requested NDC
- 67296-0140-04
- Package NDCs from labels
- 67296-0140-4, 67296-0140-2, 67296-0140-1, 67296-0140-9, 67296-0140-3, 67296-0140-04
- Manufacturer
- Redpharm Drug
- Effective date
- 2026-06-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Prednisone - Redpharm Drug | Redpharm Drug | 2026-06-12 | HUMAN PRESCRIPTION DRUG LABEL |
| Prednisone 10mg | RedPharm Drug Inc. | RedPharm Drug, Inc. | 2024-06-20 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 67296-0140-1 | 2026-01-29 | Prednisone 10mg |
| 67296-0140-2 | 2026-01-29 | Prednisone 10mg |
| 67296-0140-3 | 2026-01-29 | Prednisone 10mg |
| 67296-0140-9 | 2026-01-29 | Prednisone 10mg |
| 67296-0140-1 | 2024-06-20 | Prednisone 10mg |
| 67296-0140-2 | 2024-06-20 | Prednisone 10mg |
| 67296-0140-3 | 2024-06-20 | Prednisone 10mg |
| 67296-0140-9 | 2024-06-20 | Prednisone 10mg |
| 67296-0140-1 | 2024-01-30 | Prednisone 10mg |
| 67296-0140-2 | 2024-01-30 | Prednisone 10mg |
| 67296-0140-3 | 2024-01-30 | Prednisone 10mg |
| 67296-0140-9 | 2024-01-30 | Prednisone 10mg |
| 67296-0140-2 | 2020-04-22 | Prednisone 10mg |
| 67296-0140-2 | 2019-10-29 | Prednisone 10mg |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 67296-0140-1 | Prednisone | 10 in 1 BOTTLE | TABLET | 10 | 5 | |
| 67296-0140-2 | Prednisone | 30 in 1 BOTTLE | TABLET | 30 | 5 | |
| 67296-0140-3 | Prednisone | 42 in 1 BOTTLE | TABLET | 42 | 5 | |
| 67296-0140-9 | Prednisone | 9 in 1 BOTTLE | TABLET | 9 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 67296-0140 | PREDNISONE TABLET [REDPHARM DRUG INC.] | 5 | Current NDC, Legacy NDC, 4 package rows | 20240621_c8bc83d5-b9e2-4d31-a3df-8e899aac1ba5.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| PREDNISONE | ACTIVE INGREDIENT | VB0R961HZT | PREDNISONE TABLET [REDPHARM DRUG INC.] | 1 | |
| PREDNISONE | ACTIVE MOIETY | VB0R961HZT | PREDNISONE TABLET [REDPHARM DRUG INC.] | 1 | |
| ANHYDROUS LACTOSE | INACTIVE INGREDIENT | 3SY5LH9PMK | PREDNISONE TABLET [REDPHARM DRUG INC.] | 1 | |
| COLLOIDAL SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | PREDNISONE TABLET [REDPHARM DRUG INC.] | 1 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | PREDNISONE TABLET [REDPHARM DRUG INC.] | 1 | |
| DOCUSATE SODIUM | INACTIVE INGREDIENT | F05Q2T2JA0 | PREDNISONE TABLET [REDPHARM DRUG INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | PREDNISONE TABLET [REDPHARM DRUG INC.] | 1 | |
| SODIUM BENZOATE | INACTIVE INGREDIENT | OJ245FE5EU | PREDNISONE TABLET [REDPHARM DRUG INC.] | 1 |
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. | 6b360c1f-c862-47ee-a40e-3903c2d6162f | 2026-08-21 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| HyVee Senna S | DOCUSATE SODIUM, SENNOSIDES | HyVee Inc | 49837b2c-492f-2fed-e063-6294a90aaa24 | 2026-08-21 | Warnings | F05Q2T2JA0 |
| Senokot-S | STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM | Atlantis Consumer Healthcare, Inc. | c24cdc5e-62e0-41a6-8afb-512202a569f4 | 2026-08-21 | Warnings | F05Q2T2JA0 |
| 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 |
| Bio Combination 28 | SCHUESSLER SALTS | LDD Bioscience Private Limited | 597caf33-5107-9dec-e063-6294a90a5fcd | 2026-08-20 | Warnings | ETJ7Z6XBU4 |
| Prednisone | PREDNISONE | REMEDYREPACK INC. | 746b0bcd-122e-4ea8-a824-28415073a38e | 2026-08-20 | Warnings, Adverse reactions | 763181 312617 VB0R961HZT |
| Psorinum Complex | PHOSPHORUS, SILICEA, SULPHUR, ALOE | BioActive Nutritional, Inc. | d4746927-e6d4-463d-a084-56ffc48d1e67 | 2026-08-20 | Warnings | ETJ7Z6XBU4 |
| Prednisone | PREDNISONE | Bryant Ranch Prepack | 7ea7f6a9-78ef-42fe-baac-f817da3976fb | 2026-08-20 | Warnings, Adverse reactions | 312617 VB0R961HZT |
| Boneforce HP | CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, HEKLA LAVA, HYDROFLUORICUM ACIDUM, RHUS TOX, SILICEA, SYMPHYTUM OFFICINALE | BioActive Nutritional, Inc. | d96ca52b-781d-431c-ad2a-a54fd57eb106 | 2026-08-20 | Warnings | ETJ7Z6XBU4 |
| prednisone | PREDNISONE | Preferred Pharmaceuticals Inc. | 1e74ac55-4a48-4bf5-bfed-36c0fa37dd9f | 2026-08-19 | Warnings, Adverse reactions | 312615 VB0R961HZT |
| Foster and Thrive Senna-S Sennosides and Docusate Sodium Laxative and Stool Softener | DOCUSATE SODIUM 50MG AND SENNOSIDES 8.6MG | Strategic Sourcing Services LLC | 5966ff80-7be2-788a-e063-6294a90ab4f3 | 2026-08-19 | Warnings | F05Q2T2JA0 |
| 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 | 312617 VB0R961HZT |
| Prednisone | PREDNISONE | Major Pharmaceuticals | 57b98930-92ab-4b77-a033-ae9895ee718a | 2026-08-19 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| Stool Softener Laxative | DOCUSATE SODIUM AND SENNOSIDES | Safeway, Inc. | ae2c7300-f9c4-43b5-9f8e-30f2e7d17635 | 2026-08-19 | Warnings | F05Q2T2JA0 |
| prednisone | PREDNISONE | Preferred Pharmaceuticals Inc. | ce7663a7-4c91-4790-aa43-96f259b3bb18 | 2026-08-19 | Warnings, Adverse reactions | 198145 VB0R961HZT |
| CVS Stool Softener Fruit Punch | DOCUSATE SODIUM | CVS PHARMACY, INC | 0e6900d6-7dc9-47d6-a006-1695feb8d5a5 | 2026-08-17 | Warnings | F05Q2T2JA0 |
| Cerebellum Thalamus A Aurm | CEREBELLUM THALAMUS A AURUM | Uriel Pharmacy Inc. | e1c395b8-9221-401f-8980-c91ff8843458 | 2026-08-17 | Warnings | ETJ7Z6XBU4 |
| Stool Softener Laxative | DOCUSATE SODIUM | Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) | 306fd12b-ed60-40dc-a5be-2dc394bd29d2 | 2026-08-17 | Warnings | F05Q2T2JA0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.