NDC 50989-433 - GentaVed
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
- 50989-433
- Package NDCs from labels
- 50989-433-19, 50989-433-75, 50989-433-74
- Manufacturer
- Vedco, Inc. | Sparhawk Laboratories, Inc. | FUJIAN FUKANG PHARMACEUTICAL CO., LTD. | FARMABIOS S.p.A.
- Effective date
- 2024-12-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| GentaVed Topical Spray Gentamicin Sulfate With Betamethasone Valerate TOPICAL SPRAY | Vedco, Inc. | Sparhawk Laboratories, Inc. | FUJIAN FUKANG PHARMACEUTICAL CO., LTD. | FARMABIOS S.p.A. | 2024-12-02 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50989-433-19 | GentaVed | 60 mL in 1 BOTTLE, PUMP | SPRAY | 60 | 6 | |
| 50989-433-74 | GentaVed | 240 mL in 1 BOTTLE, PUMP | SPRAY | 240 | 6 | |
| 50989-433-75 | GentaVed | 120 mL in 1 BOTTLE, PUMP | SPRAY | 120 | 6 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| BETAMETHASONE VALERATE | ACTIVE INGREDIENT | 9IFA5XM7R2 | GENTAVED (GENTAMICIN SULFATE) SPRAY [VEDCO, INC.] | 1 | |
| GENTAMICIN SULFATE | ACTIVE INGREDIENT | 8X7386QRLV | GENTAVED (GENTAMICIN SULFATE) SPRAY [VEDCO, INC.] | 1 | |
| BETAMETHASONE | ACTIVE MOIETY | 9842X06Q6M | GENTAVED (GENTAMICIN SULFATE) SPRAY [VEDCO, INC.] | 1 | |
| GENTAMICIN | ACTIVE MOIETY | T6Z9V48IKG | GENTAVED (GENTAMICIN SULFATE) SPRAY [VEDCO, 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.