NDC 86036-014 - Crizotinib
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
- 86036-014
- Package NDCs from labels
- 86036-014-00
- Manufacturer
- Nanjing Chemlin Biomedical Science & Technology Co, Ltd.
- Effective date
- 2022-10-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Crizotinib | Nanjing Chemlin Biomedical Science & Technology Co, Ltd. | 2022-10-25 | BULK INGREDIENT - ANIMAL DRUG |
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 |
|---|---|---|---|---|---|---|
| Xalkori | CRIZOTINIB | Pfizer Laboratories Div Pfizer Inc | 2a51b0de-47d6-455e-a94c-d2c737b04ff7 | 2025-07-22 | Warnings, Adverse reactions | 53AH36668S |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.