NDC 63069-401 - METVIXIA
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
- 63069-401
- Package NDCs from labels
- 63069-401-01
- Manufacturer
- Penn Pharmaceutical Services Ltd.
- Effective date
- 2007-09-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| METVIXIA - Penn Pharmaceutical Services Ltd. | Penn Pharmaceutical Services Ltd. | 2007-09-26 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63069-401-01 | METVIXIA | 2 g in 1 TUBE | CREAM | 2 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| 3F324924-DA9E-E915-4D3F-50AFC030F0D4 | d02af310-d097-4886-86e5-adcf6bca0533 | 2007-09-26 | Warnings, Adverse reactions | 3F324924-DA9E-E915-4D3F-50AFC030F0D4 d02af310-d097-4886-86e5-adcf6bca0533 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.