NDC 73309-016 - Rifabutin
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
- 73309-016
- Package NDCs from labels
- 73309-016-01
- Manufacturer
- BLUEBAY SHANDONG CO.,LTD
- Effective date
- 2019-08-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Rifabutin - BLUEBAY SHANDONG CO.,LTD | BLUEBAY SHANDONG CO.,LTD | 2019-08-19 | BULK INGREDIENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73309-016-01 | Rifabutin | 50 g in 1 JAR | POWDER | 50 | 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 |
|---|---|---|---|---|---|---|
| Rifabutin | RIFABUTIN | REMEDYREPACK INC. | 25a60937-cbbe-4a50-994f-2ce15203f589 | 2026-09-01 | Warnings, Adverse reactions | 1W306TDA6S |
| Rifabutin | RIFABUTIN | Mylan Pharmaceuticals Inc. | c2026b67-4755-4236-96b6-a6b5e7399707 | 2026-07-20 | Warnings, Adverse reactions | 1W306TDA6S |
| Rifabutin | RIFABUTIN | REMEDYREPACK INC. | 754d2d7f-f0db-4f89-8fcd-5e2ff52d5030 | 2026-06-05 | Warnings, Adverse reactions | 1W306TDA6S |
| Rifabutin | RIFABUTIN | i3 Pharmaceuticals, LLC | fd6062e2-17c8-48f4-a1fe-69ebe410f583 | 2026-02-20 | Warnings, Adverse reactions | 1W306TDA6S |
| Talicia | OMEPRAZOLE MAGNESIUM, AMOXICILLIN AND RIFABUTIN | RedHill Biopharma Ltd | 68c4e9dc-dbcf-4151-b6f7-5e4b9922b76f | 2025-12-23 | Warnings, Adverse reactions | 1W306TDA6S |
| Rifabutin | RIFABUTIN | Marlex Pharmaceuticals, Inc. | df7d4103-42e4-4e4f-e053-2a95a90a8ce8 | 2025-11-18 | Warnings, Adverse reactions | 1W306TDA6S |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.