NDC 62022-712 - CODRIX
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
- 62022-712
- Package NDCs from labels
- 62022-712-01, 62022-712-05, 62022-712-50
- Manufacturer
- Andrx Laboratories, Inc.
- Effective date
- 2008-04-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CODRIX™ (Acetaminophen and Codeine Phosphate Tablets, USP) | Andrx Laboratories, Inc. | 2008-04-25 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62022-712-01 | CODRIX | 100 in 1 BOTTLE | TABLET | 100 | 3 | |
| 62022-712-05 | CODRIX | 500 in 1 BOTTLE | TABLET | 500 | 3 | |
| 62022-712-50 | CODRIX | 1000 in 1 BOTTLE | TABLET | 1000 | 3 |
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 |
|---|---|---|---|---|---|---|
| A99F028B-C093-025A-CD5E-46D71C2D44B2 | b7c4c175-d3f9-4ed8-abb8-cfb33b9dc2b3 | 2008-04-25 | Warnings, Adverse reactions | A99F028B-C093-025A-CD5E-46D71C2D44B2 b7c4c175-d3f9-4ed8-abb8-cfb33b9dc2b3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.