NDC 73377-136-01 - Lufenuron
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
- 73377-136
- Requested NDC
- 73377-136-01
- Package NDCs from labels
- 73377-136-01, 73377-136-02, 73377-136-03
- Manufacturer
- AX Pharmaceutical Corp
- Effective date
- 2024-11-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lufenuron - AX Pharmaceutical Corp | AX Pharmaceutical Corp | 2024-11-28 | BULK INGREDIENT - ANIMAL DRUG |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73377-136-01 | Lufenuron | 5 kg in 1 DRUM | POWDER | 5 | 3 | |
| 73377-136-02 | Lufenuron | 1 kg in 1 JAR | POWDER | 1 | 3 | |
| 73377-136-03 | Lufenuron | 0.5 kg in 1 JAR | POWDER | 0.5 | 3 |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.