NDC 72205-166-11 - 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
- 72205-166
- Requested NDC
- 72205-166-11
- Package NDCs from labels
- 72205-166-30, 72205-166-90, 72205-166-11, 72205-166-99, 72205-166-66
- Manufacturer
- Novadoz Pharmaceuticals LLC | MSN LABORATORIES PRIVATE LIMITED
- Effective date
- 2023-11-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OLMESARTAN - Novadoz Pharmaceuticals LLC | MSN LABORATORIES PRIVATE LIMITED | Novadoz Pharmaceuticals LLC | MSN LABORATORIES PRIVATE LIMITED | 2023-11-30 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72205-166-11 | Olmesartan medoxomil | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 2 | |
| 72205-166-30 | Olmesartan medoxomil | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 2 | |
| 72205-166-66 | Olmesartan medoxomil | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | 2 | |
| 72205-166-90 | Olmesartan medoxomil | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 2 | |
| 72205-166-99 | Olmesartan medoxomil | 10 in 1 CARTON | TABLET, FILM COATED | 10 | 2 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72205-166-30 | EA - Each | 72205-166 | 709f6715-1cde-46a7-95f8-5ed3363cf68a | 1 | 2024-08-12 |
| 72205-166-66 | EA - Each | 72205-166 | c08239dd-56b8-40c5-84ef-4935bfa009de | 1 | 2024-08-12 |
| 72205-166-90 | EA - Each | 72205-166 | 00161ba1-c8d7-451c-ad6c-30575f447f46 | 1 | 2024-08-12 |
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.