NDC 73377-009-07 - Tacrolimus
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
- 73377-009
- Requested NDC
- 73377-009-07
- Package NDCs from labels
- 73377-009-01, 73377-009-02, 73377-009-03, 73377-009-04, 73377-009-05, 73377-009-06, 73377-009-07
- Manufacturer
- AX Pharmaceutical Corp
- Effective date
- 2026-09-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Tacrolimus - AX Pharmaceutical Corp | AX Pharmaceutical Corp | 2026-09-30 | BULK INGREDIENT - ANIMAL DRUG |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73377-009-01 | Tacrolimus | 50 g in 1 JAR | POWDER | 50 | 6 | |
| 73377-009-02 | Tacrolimus | 10 g in 1 JAR | POWDER | 10 | 6 | |
| 73377-009-03 | Tacrolimus | 1 g in 1 JAR | POWDER | 1 | 6 | |
| 73377-009-04 | Tacrolimus | 3.5 g in 1 JAR | POWDER | 3.5 | 6 | |
| 73377-009-05 | Tacrolimus | 6.7 g in 1 JAR | POWDER | 6.7 | 6 | |
| 73377-009-06 | Tacrolimus | 100 g in 1 JAR | POWDER | 100 | 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Prograf | TACROLIMUS | Astellas Pharma US, Inc. | 7f667de1-9dfa-4bd6-8ba0-15ee2d78873b | 2023-08-25 | Boxed warning, Warnings, Adverse reactions | WM0HAQ4WNM |
| Tacrolimus | TACROLIMUS | Padagis Israel Pharmaceuticals Ltd | 6b601eaf-4f3a-4a8b-8cd8-1000defa9822 | 2021-11-15 | Warnings, Adverse reactions | WM0HAQ4WNM |
| Tacrolimus | TACROLIMUS | Aphena Pharma Solutions - Tennessee, LLC | 4caa20af-45a8-4365-9f06-1568afae61b1 | 2017-05-03 | Boxed warning, Warnings, Adverse reactions | WM0HAQ4WNM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.