NDC 11026-2632 - Obstetrix EC
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
- 11026-2632
- Package NDCs from labels
- 11026-2632-6
- Manufacturer
- Seyer Pharmatec, Inc.
- Effective date
- 2023-02-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Obstetrix™ EC | Seyer Pharmatec, Inc. | 2023-02-14 | DIETARY SUPPLEMENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11026-2632-6 | Obstetrix EC | 60 in 1 BOTTLE | TABLET | 60 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11026-2632 | OBSTETRIX EC (BETA CAROTENE, ASCORBIC ACID, CHOLECALCIFEROL, DL-ALPHA TOCOPHERYL ACETATE, THIAMINE HYDROCHLORIDE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, L-5-METHYLTETRAHYDROFOLATE CALCIUM, CYANOCOBALAMIN, CARBONYL IRON, MAGNESIUM OXIDE, ZINC OXIDE, SODIUM SELENATE) TABLET [SEYER PHARMATEC, INC.] | 1 | 1 package rows | 20230224_a2506c4b-63d2-4b55-930e-15f74c1637cc.zip |
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.