NDC 0049-5600 - Atarax
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
- 0049-5600
- Package NDCs from labels
- 0049-5600-66
- Manufacturer
- Roerig
- Effective date
- 2006-06-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Atarax - Roerig | Roerig | 2006-06-20 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0049-5600-66 | Atarax | 100 in 1 BOTTLE | TABLET | 100 | 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 |
|---|---|---|---|---|---|---|
| 7EAF5043-5C73-47AF-904B-8E1FAE02AF2E | 7EAF5043-5C73-47AF-904B-8E1FAE02AF2E | 2006-06-20 | Warnings, Adverse reactions | 7EAF5043-5C73-47AF-904B-8E1FAE02AF2E 7EAF5043-5C73-47AF-904B-8E1FAE02AF2E |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.