NDC 55111-643-79 - Omeprazole
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
- 55111-643
- Requested NDC
- 55111-643-79
- Package NDCs from labels
- 55111-643-30, 55111-643-01, 55111-643-05, 55111-643-79, 55111-643-78
- Manufacturer
- Proficient Rx LP
- Effective date
- 2026-08-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Omeprazole - Proficient Rx LP | Proficient Rx LP | 2026-08-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Omeprazole - Dr. Reddy's Laboratories Limited | Dr. Reddy's Laboratories Limited - FTO III | Dr. Reddy's Laboratories Limited | Dr. Reddy's Laboratories Limited - FTO III | 2026-03-02 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55111-643-01 | Omeprazole | 100 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 100 | 34 | |
| 55111-643-05 | Omeprazole | 500 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 500 | 34 | |
| 55111-643-30 | Omeprazole | 30 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 30 | 34 | |
| 55111-643-78 | Omeprazole | 10 in 1 CARTON | CAPSULE, DELAYED RELEASE | 10 | 34 | |
| 55111-643-79 | Omeprazole | 10 in 1 BLISTER PACK | CAPSULE, DELAYED RELEASE | 10 | 34 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55111-643-01 | EA - Each | 55111-643 | 494e577b-97a6-4012-afd1-f4208307ef88 | 1 | 2026-03-17 |
| 55111-643-30 | EA - Each | 55111-643 | 144bd8d5-7399-43a1-bdf3-74516a41819c | 1 | 2026-03-17 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.