NDC 54771-2012 - Synovex One
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
- 54771-2012
- Package NDCs from labels
- 54771-2012-1
- Manufacturer
- Zoetis Inc.
- Effective date
- 2026-06-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SYNOVEX ® ONE GROWER | Zoetis Inc. | 2026-06-12 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54771-2012-1 | Synovex One | 10 in 1 CARTON | IMPLANT | 10 | 2 | |
| 54771-2012-1 | Synovex One | 10 in 1 CARTRIDGE | IMPLANT | 10 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 54771-2012 | SYNOVEX ONE (TRENBOLONE ACETATE AND ESTRADIOL BENZOATE) IMPLANT [ZOETIS INC.] | 2 | 2 package rows | 20211110_aaac6cde-7622-4c33-aff5-718a303066a4.zip |
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 |
|---|---|---|---|---|---|---|
| Solvent/Small Ring Combination 9317 | SOLVENT/SMALL RING COMBINATION | Professional Complementary Health Formulas | 01a1b313-3edb-4907-9d9b-bb1d1061b4ef | 2026-01-08 | Warnings | 1S4CJB5ZGN |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.