NDC 69238-2675-01 - Amlodipine and Olmesartan Medoxomil
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
- 69238-2675
- Requested NDC
- 69238-2675-01
- Package NDCs from labels
- 69238-2675-1, 69238-2675-01
- Manufacturer
- AvKARE
- Effective date
- 2026-01-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Amlodipine and Olmesartan Medoxomil - AvKARE | AvKARE | 2026-01-13 | HUMAN PRESCRIPTION DRUG LABEL |
| AMLODIPINE - Amneal Pharmaceuticals NY LLC | ScieGen Pharmaceuticals, Inc | Amneal Pharmaceuticals NY LLC | ScieGen Pharmaceuticals, Inc | 2024-03-26 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69238-2675-1 | Amlodipine and Olmesartan Medoxomil | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69238-2675 | AMLODIPINE AND OLMESARTAN MEDOXOMIL TABLET, FILM COATED [AMNEAL PHARMACEUTICALS NY LLC] | 1 | Current NDC, 1 package rows | 20240502_02f9b562-6f7f-4783-bb0d-67c318073e1c.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.