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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Omeprazole | OMEPRAZOLE | PHOENIX RX LLC | 3b19d724-821b-61dc-e063-6294a90aa4d3 | 2025-07-29 | Warnings, Adverse reactions | ANDA078490 198051 KG60484QX9 |
| Systane COMPLETE PF | PROPYLENE GLYCOL | Alcon Laboratories, Inc. | 99b63d62-1cf0-4f28-8760-773917c2538a | 2025-07-29 | Warnings | 6DC9Q167V3 |
| Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Kenvue Brands LLC | 003123d2-9675-fdd2-e063-6294a90a0130 | 2025-07-28 | Warnings | 15FIX9V2JP |
| Neutrogena Mineral Ultra Sheer Face SPF 70 | TITANIUM DIOXIDE, ZINC OXIDE | Kenvue Brands LLC | 20e0badf-fe25-1d27-e063-6294a90a7cfe | 2025-07-28 | Warnings | 15FIX9V2JP |
| Omeprazole Magnesium | OMEPRAZOLE MAGNESIUM | Gericare Pharmaceuticals | 0e1f5d7c-5956-3be7-e054-00144ff8d46c | 2025-07-28 | Warnings | 198051 |
| Dolce and Gabbana Everlast Foundation SPF 20 01N Light | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 2ccf4e45-4cec-417d-9f4c-28f376025f1d | 2025-07-25 | Warnings | 15FIX9V2JP |
| Sunscreen | TITANIUM DIOXIDE 6.8% | Baxter of California, LLC | 146030bc-2bf4-25ea-e063-6294a90a4613 | 2025-07-24 | Warnings | 15FIX9V2JP |
| Omeprazole Magnesium | OMEPRAZOLE MAGNESIUM | HEB | 5d8b3f5f-f680-64ae-b360-c0bd06b2ac92 | 2025-07-23 | Warnings | 198051 |
| Omeprazole Magnesium | OMEPRAZOLE MAGNESIUM | CVS Health Corp. | 3bbfa87d-f8b7-19bd-9f12-39cba31ae0b3 | 2025-07-23 | Warnings | 198051 |
| Omeprazole | OMEPRAZOLE | PHOENIX RX LLC | 3a9baece-03be-6c77-e063-6394a90a7032 | 2025-07-23 | Warnings, Adverse reactions | 198051 KG60484QX9 |
| Omeprazole Magnesium | OMEPRAZOLE MAGNESIUM | Chain Drug Marketing Association | ab5d339b-2c02-611d-d5db-8e1891684fe0 | 2025-07-23 | Warnings | 198051 |
| Acid Reducer | OMEPRAZOLE MAGNESIUM | LEADER/ Cardinal Health 110, Inc. | 1dc00f13-d1f5-15a0-32cc-4fc041865e72 | 2025-07-23 | Warnings | 198051 |
| Omeprazole Magnesium | OMEPRAZOLE MAGNESIUM | Albertsons Companies | 302b1332-181b-834b-4154-d849cb3a1ef0 | 2025-07-23 | Warnings | 198051 |
| Omeprazole Magnesium | OMEPRAZOLE MAGNESIUM | Discount Drug Mart, Inc | daeeba93-29d5-efb4-a591-3e72c4e50341 | 2025-07-23 | Warnings | 198051 |
| Omeprazole Magnesium | OMEPRAZOLE MAGNESIUM 20.6MG CAPSULES | The Kroger Co. | 8a6bbc31-7c50-a730-4233-e346fd7eb5ba | 2025-07-22 | Warnings | 198051 |
| Omeprazole Magnesium | OMEPRAZOLE MAGNESIUM | Dr. Reddy's Laboratories Inc. | fe0eb905-2042-aed1-a67d-a219e76f679b | 2025-07-22 | Warnings | 198051 |
| Omeprazole Magnesium | OMEPRAZOLE MAGNESIUM | Walgreens Company | ee8b1740-9bcf-5b70-bd8d-97f98303dc72 | 2025-07-22 | Warnings | 198051 |
| Omeprazole Magnesium | OMEPRAZOLE MAGNESIUM 20.6MG CAPSULES | Wal-Mart Stores Inc | 3160e212-9ee9-8316-f51e-4628862f654c | 2025-07-22 | Warnings | 198051 |
| Omeprazole Magnesium | OMEPRAZOLE MAGNESIUM | Chain Drug Consortium, LLC | 39ac65c0-d957-125f-f00b-e3846a437489 | 2025-07-22 | Warnings | 198051 |
| Omeprazole Magnesium | OMEPRAZOLE MAGNESIUM | Chain Drug Marketing Association | fdf1259b-e9d3-70a9-c209-e2eb6b152841 | 2025-07-22 | Warnings | 198051 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.