NDC 73309-317 - Trazodone HCl
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
- 73309-317
- Package NDCs from labels
- 73309-317-01, 73309-317-02
- Manufacturer
- BLUEBAY SHANDONG CO.,LTD
- Effective date
- 2021-09-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Trazodone HCl - BLUEBAY SHANDONG CO.,LTD | BLUEBAY SHANDONG CO.,LTD | 2021-09-22 | BULK INGREDIENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73309-317-01 | Trazodone HCl | 100 g in 1 JAR | POWDER | 100 | 1 | |
| 73309-317-02 | Trazodone HCl | 1000 g in 1 JAR | POWDER | 1000 | 1 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Trazodone Hydrochloride | TRAZODONE HYDROCHLORIDE | Proficient Rx LP | f6c3fb84-5b68-4675-a853-fe49bfbf3f9f | 2022-06-01 | Boxed warning, Warnings, Adverse reactions | 6E8ZO8LRNM |
| Trazodone Hydrochloride | TRAZODONE HYDROCHLORIDE | Proficient Rx LP | 2a1d0989-6ed5-4a2f-bd03-73d61eb40232 | 2022-06-01 | Boxed warning, Warnings, Adverse reactions | 6E8ZO8LRNM |
| Trazodone Hydrochloride | TRAZODONE HYDROCHLORIDE | Aphena Pharma Solutions - Tennessee, LLC | 5d22a06c-9cb8-4b49-8d67-769d181ad70c | 2021-03-10 | Boxed warning, Warnings, Adverse reactions | 6E8ZO8LRNM |
| Trazodone Hydrochloride | TRAZODONE HYDROCHLORIDE | Teva Pharmaceuticals USA, Inc. | 9c4da6ad-d4d1-4e8c-918d-8ac48512a93f | 2020-06-30 | Boxed warning, Warnings, Adverse reactions | 6E8ZO8LRNM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.