NDC 10144-920 - Qutenza
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
- 10144-920
- Package NDCs from labels
- 10144-920-00
- Manufacturer
- Acorda Therapeutics, Inc. | Sharp Corporation | Contract Pharmaceuticals Limited Canada - Lab Svcs (CPL) | SGS Life Science Services | Exova Canada Inc. | Contract Pharmaceuticals Limited Canada (CPL) | SGS Institut Fresenius GmbH | Lohmann Therapie-Systeme AG (LTS) (Germany)
- Effective date
- 2018-11-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Qutenza | Acorda Therapeutics, Inc. | Sharp Corporation | Contract Pharmaceuticals Limited Canada - Lab Svcs (CPL) | SGS Life Science Services | Exova Canada Inc. | Contract Pharmaceuticals Limited Canada (CPL) | SGS Institut Fresenius GmbH | Lohmann Therapie-Systeme AG (LTS) (Germany) | 2018-11-05 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| capsaicin | ACTIVE INGREDIENT | S07O44R1ZM | QUTENZA (CAPSAICIN) KIT [ACORDA THERAPEUTICS, INC.] | 1 | |
| capsaicin | ACTIVE MOIETY | S07O44R1ZM | QUTENZA (CAPSAICIN) KIT [ACORDA THERAPEUTICS, INC.] | 1 | |
| diethylene glycol monoethyl ether | INACTIVE INGREDIENT | A1A1I8X02B | QUTENZA (CAPSAICIN) KIT [ACORDA THERAPEUTICS, INC.] | 1 | |
| dimethicone | INACTIVE INGREDIENT | 92RU3N3Y1O | QUTENZA (CAPSAICIN) KIT [ACORDA THERAPEUTICS, INC.] | 1 | |
| ethylcelluloses | INACTIVE INGREDIENT | 7Z8S9VYZ4B | QUTENZA (CAPSAICIN) KIT [ACORDA THERAPEUTICS, INC.] | 1 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.