NDC 65628-271 - Konvomep
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
- 65628-271
- Package NDCs from labels
- 65628-271-03, 65628-271-05, 65628-271-10
- Manufacturer
- Azurity Pharmaceuticals, Inc.
- Effective date
- 2025-12-16
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Konvomep - Azurity Pharmaceuticals, Inc. | Azurity Pharmaceuticals, Inc. | 2025-12-16 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 65628-271-03 | Konvomep | 90 mL in 1 BOTTLE | SOLUTION | 90 mL | 84 mg in 1mL | 6 |
| 65628-271-05 | Konvomep | 150 mL in 1 BOTTLE | SOLUTION | 150 mL | 84 mg in 1mL | 6 |
| 65628-271-10 | Konvomep | 300 mL in 1 BOTTLE | SOLUTION | 300 mL | 84 mg in 1mL | 6 |
DailyMed Dashboard NDC Coverage#
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.