Application 050581
- Type
- NDA
- Sponsor
- MERCK
Application Products#
| Product | Drug | Ingredient | Form | Strength | Reference drug | Reference standard |
|---|---|---|---|---|---|---|
| 001 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | CEFOXITIN SODIUM | INJECTABLE;INJECTION | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | Yes | No |
| 002 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | CEFOXITIN SODIUM | INJECTABLE;INJECTION | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | Yes | No |
| 003 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | CEFOXITIN SODIUM | INJECTABLE;INJECTION | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | Yes | No |
| 004 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | CEFOXITIN SODIUM | INJECTABLE;INJECTION | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | Yes | No |
Orange Book products#
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| N050581-001 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | CEFOXITIN SODIUM | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | |
| N050581-002 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | CEFOXITIN SODIUM | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | |
| N050581-003 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | CEFOXITIN SODIUM | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | |
| N050581-004 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | CEFOXITIN SODIUM | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 |
Observed Orange Book product history#
Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2024-03-16 18:09 UTC · 4 captures of this ZIP | 2024-03 | N050581-001 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 6a51e52b5d6a… | |
| 2024-03-16 18:09 UTC · 4 captures of this ZIP | 2024-03 | N050581-002 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 6a51e52b5d6a… | |
| 2024-03-16 18:09 UTC · 4 captures of this ZIP | 2024-03 | N050581-003 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 6a51e52b5d6a… | |
| 2024-03-16 18:09 UTC · 4 captures of this ZIP | 2024-03 | N050581-004 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 6a51e52b5d6a… | |
| 2024-02-18 07:12 UTC | 2024-02 | N050581-001 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 1c564ffb4f44… | |
| 2024-02-18 07:12 UTC | 2024-02 | N050581-002 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 1c564ffb4f44… | |
| 2024-02-18 07:12 UTC | 2024-02 | N050581-003 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 1c564ffb4f44… | |
| 2024-02-18 07:12 UTC | 2024-02 | N050581-004 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 1c564ffb4f44… | |
| 2023-12-20 04:57 UTC | 2023-12 | N050581-001 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | ea1830bbd6c7… | |
| 2023-12-20 04:57 UTC | 2023-12 | N050581-002 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | ea1830bbd6c7… | |
| 2023-12-20 04:57 UTC | 2023-12 | N050581-003 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | ea1830bbd6c7… | |
| 2023-12-20 04:57 UTC | 2023-12 | N050581-004 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | ea1830bbd6c7… | |
| 2023-11-28 05:40 UTC · 2 captures of this ZIP | 2023-11 | N050581-001 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | a72a2bbeb626… | |
| 2023-11-28 05:40 UTC · 2 captures of this ZIP | 2023-11 | N050581-002 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | a72a2bbeb626… | |
| 2023-11-28 05:40 UTC · 2 captures of this ZIP | 2023-11 | N050581-003 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | a72a2bbeb626… | |
| 2023-11-28 05:40 UTC · 2 captures of this ZIP | 2023-11 | N050581-004 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | a72a2bbeb626… | |
| 2023-10-25 00:34 UTC · 2 captures of this ZIP | 2023-10 | N050581-001 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 9b2671bbb829… | |
| 2023-10-25 00:34 UTC · 2 captures of this ZIP | 2023-10 | N050581-002 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 9b2671bbb829… | |
| 2023-10-25 00:34 UTC · 2 captures of this ZIP | 2023-10 | N050581-003 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 9b2671bbb829… | |
| 2023-10-25 00:34 UTC · 2 captures of this ZIP | 2023-10 | N050581-004 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 9b2671bbb829… | |
| 2023-07-15 15:27 UTC · 2 captures of this ZIP | 2023-07 | N050581-001 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | a67488948f0b… | |
| 2023-07-15 15:27 UTC · 2 captures of this ZIP | 2023-07 | N050581-002 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | a67488948f0b… | |
| 2023-07-15 15:27 UTC · 2 captures of this ZIP | 2023-07 | N050581-003 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | a67488948f0b… | |
| 2023-07-15 15:27 UTC · 2 captures of this ZIP | 2023-07 | N050581-004 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | a67488948f0b… | |
| 2023-06-13 01:57 UTC · 3 captures of this ZIP | 2023-06 | N050581-001 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 3f0d92c62455… | |
| 2023-06-13 01:57 UTC · 3 captures of this ZIP | 2023-06 | N050581-002 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 3f0d92c62455… | |
| 2023-06-13 01:57 UTC · 3 captures of this ZIP | 2023-06 | N050581-003 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 3f0d92c62455… | |
| 2023-06-13 01:57 UTC · 3 captures of this ZIP | 2023-06 | N050581-004 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 3f0d92c62455… | |
| 2023-05-13 08:27 UTC | 2023-05 | N050581-001 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 053a50430f4f… | |
| 2023-05-13 08:27 UTC | 2023-05 | N050581-002 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 053a50430f4f… | |
| 2023-05-13 08:27 UTC | 2023-05 | N050581-003 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 053a50430f4f… | |
| 2023-05-13 08:27 UTC | 2023-05 | N050581-004 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 053a50430f4f… | |
| 2023-01-26 05:58 UTC | 2023-01 | N050581-001 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 3bdfa0b2c4d7… | |
| 2023-01-26 05:58 UTC | 2023-01 | N050581-002 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 3bdfa0b2c4d7… | |
| 2023-01-26 05:58 UTC | 2023-01 | N050581-003 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 3bdfa0b2c4d7… | |
| 2023-01-26 05:58 UTC | 2023-01 | N050581-004 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 3bdfa0b2c4d7… | |
| 2022-11-12 20:34 UTC · 5 captures of this ZIP | 2022-11 | N050581-001 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 3a93d1ddd44b… | |
| 2022-11-12 20:34 UTC · 5 captures of this ZIP | 2022-11 | N050581-002 | MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 3a93d1ddd44b… | |
| 2022-11-12 20:34 UTC · 5 captures of this ZIP | 2022-11 | N050581-003 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 3a93d1ddd44b… | |
| 2022-11-12 20:34 UTC · 5 captures of this ZIP | 2022-11 | N050581-004 | MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER | EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE / INJECTION | RLD | 1984-09-20 | 3a93d1ddd44b… |
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 |
|---|---|---|---|---|---|---|
| Cefoxitin | CEFOXITIN SODIUM | Fresenius Kabi USA, LLC | 2a9d1e7b-96ee-4e6c-a1e8-47b76b924422 | 2023-07-10 | Warnings, Adverse reactions | CEFOXITIN SODIUM |
| Cefoxitin | CEFOXITIN SODIUM | Fresenius Kabi USA, LLC | d02170ff-65aa-48b8-a922-94271c46ffa7 | 2022-09-23 | Warnings, Adverse reactions | CEFOXITIN SODIUM |
| Cefoxitin and Dextrose | CEFOXITIN SODIUM | B. Braun Medical Inc. | 6c7e9485-1ede-411c-8c46-911439332864 | 2019-07-29 | Warnings, Adverse reactions | CEFOXITIN SODIUM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Documents#
| Document | Submission type | Date |
|---|---|---|
| 42650 | SUPPL | 2004-08-10 |