NDC 73309-156-01 - Pyrazinamide
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
- 73309-156
- Requested NDC
- 73309-156-01
- Package NDCs from labels
- 73309-156-01
- Manufacturer
- BLUEBAY SHANDONG CO.,LTD
- Effective date
- 2020-07-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Pyrazinamide - BLUEBAY SHANDONG CO.,LTD | BLUEBAY SHANDONG CO.,LTD | 2020-07-02 | BULK INGREDIENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73309-156-01 | Pyrazinamide | 1 kg in 1 BAG | POWDER | 1 | 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 |
|---|---|---|---|---|---|---|
| Pyrazinamide | PYRAZINAMIDE | ANI Pharmaceuticals, Inc. | 262d8829-728c-48db-b89b-88d13b87e684 | 2026-03-02 | Warnings, Adverse reactions | 2KNI5N06TI |
| PYRAZINAMIDE | PYRAZINAMIDE TABLET | MARLEX PHARMACEUTICALS, INC | db250a85-2e20-87e9-e053-2a95a90a72b6 | 2025-12-04 | Warnings, Adverse reactions | 2KNI5N06TI |
| Pyrazinamide | PYRAZINAMIDE | American Health Packaging | e2dbbdf9-ddfd-4d6d-ad42-6e658969f11e | 2025-11-13 | Warnings, Adverse reactions | 2KNI5N06TI |
| pyrazinamide | PYRAZINAMIDE | Hikma Pharmaceuticals USA Inc | 566db230-3d73-482f-b67d-defd0b2dc46c | 2023-10-03 | Warnings, Adverse reactions | 2KNI5N06TI |
| Pyrazinamide | PYRAZINAMIDE | Macleods Pharmaceuticals Limited | a8b7ba02-8509-475b-8a3b-39d205af3f1e | 2022-12-06 | Warnings, Adverse reactions | 2KNI5N06TI |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.