NDC 80425-0071-01 - Omeprazole DR
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
- 80425-0071
- Requested NDC
- 80425-0071-01
- Package NDCs from labels
- 80425-0071-3, 80425-0071-2, 80425-0071-1, 80425-0071-01
- Manufacturer
- Advanced Rx of Tennessee, LLC
- Effective date
- 2024-12-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Omeprazole DR - Advanced Rx of Tennessee, LLC | Advanced Rx of Tennessee, LLC | 2024-12-31 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80425-0071-1 | OmeprazoleDR | 30 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 30 | 9 | |
| 80425-0071-2 | OmeprazoleDR | 60 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 60 | 9 | |
| 80425-0071-3 | OmeprazoleDR | 120 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 120 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 80425-0071 | OMEPRAZOLE DR (OMEPRAZOLE) CAPSULE, DELAYED RELEASE [ADVANCED RX OF TENNESSEE, LLC] | 9 | Current NDC, Legacy NDC, 3 package rows | 20250108_af85e324-ef9f-196c-e053-2995a90a384e.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 80425-0071-1 | EA - Each | 80425-0071 | 4d54795a-131a-485d-85c4-dd4738c2028c | 1 | 2023-04-07 |
| 80425-0071-2 | EA - Each | 80425-0071 | 81d3a7ee-0a1a-48c6-a31d-8da356384752 | 1 | 2023-04-07 |
| 80425-0071-3 | EA - Each | 80425-0071 | 8820d579-6cc6-4d02-ac40-68b408fcb38e | 1 | 2023-04-07 |
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 | Rite Aid Corporation | 28a0b4c8-3ad3-451c-a957-28aef5e3d8b5 | 2026-09-09 | Warnings | KG60484QX9 |
| Omeprazole | OMEPRAZOLE | Amazon.com Services LLC | 94faa721-e925-4033-8661-d1990dfa920d | 2026-08-30 | Warnings | KG60484QX9 |
| Omeprazole | OMEPRAZOLE | REMEDYREPACK INC. | 63b3982a-b541-4b0d-99d4-93a673e57d46 | 2026-08-28 | Warnings, Adverse reactions | 198051 KG60484QX9 |
| omeprazole and sodium bicarbonate | OMEPRAZOLE, SODIUM BICARBONATE | Amazon.com Services LLC | bb453f26-c7df-4cce-8793-337cb5d5f9a9 | 2026-08-19 | Warnings | KG60484QX9 |
| good now omeprazole | OMEPRAZOLE | Gobrands, Inc | 0e7c4aee-2c9f-4d5c-9d47-c333bf00ba9f | 2026-08-19 | Warnings | KG60484QX9 |
| Omeprazole | OMEPRAZOLE | Discount Drug Mart, Inc | 4d5f30c2-775d-a1a3-e063-6394a90a07ff | 2026-08-12 | Warnings | KG60484QX9 |
| GoodMeds 24HR Acid Reducer Omeprazole 20mg | OMEPRAZOLE 20MG | Cabinet Health P.B.C. | 58c9c8ef-b929-14eb-e063-6294a90a3761 | 2026-08-11 | Warnings | KG60484QX9 |
| OMEPRAZOLE | OMEPRAZOLE | H E B | 4eb05eb3-be59-4132-95a8-5a8f5065d758 | 2026-08-10 | Warnings | 198051 KG60484QX9 |
| Omeprazole | OMEPRAZOLE | REMEDYREPACK INC. | ded0df8b-1813-4595-ac2b-5499704bfd48 | 2026-08-05 | Warnings, Adverse reactions | 198051 KG60484QX9 |
| Omeprazole | OMEPRAZOLE | A-S Medication Solutions | 6ea9a6f3-b756-4cdf-b3db-f666a2c17d66 | 2026-08-04 | Warnings, Adverse reactions | 198051 KG60484QX9 |
| Omeprazole | OMEPRAZOLE | Proficient Rx LP | 062800b1-790a-41c3-a8be-94143d2c7fb6 | 2026-08-01 | Warnings, Adverse reactions | KG60484QX9 |
| Omeprazole | OMEPRAZOLE | PD-Rx Pharmaceuticals, Inc. | 96104ea6-c08f-40b5-83f5-d840b317f1fd | 2026-07-31 | Warnings, Adverse reactions | 198051 KG60484QX9 |
| Omeprazole | OMEPRAZOLE | REMEDYREPACK INC. | a19ce586-59b7-4c2e-9e8d-12e8f0f058e2 | 2026-07-21 | Warnings, Adverse reactions | 198051 KG60484QX9 |
| Omeprazole | OMEPRAZOLE | PD-Rx Pharmaceuticals, Inc. | 0344268f-d8e6-48d5-b1e1-f750ed1d8a52 | 2026-07-17 | Warnings, Adverse reactions | KG60484QX9 |
| Omeprazole | OMEPRAZOLE | HAWAII REPACK, INC. | 9359e826-5263-44fc-8dd3-9d0852fe42d6 | 2026-07-13 | Warnings, Adverse reactions | 198051 KG60484QX9 |
| Omeprazole | OMEPRAZOLE | Bryant Ranch Prepack | dcaadc8c-32d1-476f-b821-973c012b7fa7 | 2026-07-10 | Warnings, Adverse reactions | 198051 KG60484QX9 |
| careone omeprazole | OMEPRAZOLE | American Sales Company | 5b88717a-e90c-4e74-ae2a-29270e14a3cc | 2026-07-08 | Warnings | KG60484QX9 |
| Omeprazole | OMEPRAZOLE MAGNESIUM | YYBA CORP | 535c2543-84f3-f5c1-e063-6394a90adb1e | 2026-07-07 | Warnings | 198051 |
| Omeprazole | OMEPRAZOLE | St. Mary's Medical Park Pharmacy | 4c0cf466-f9e8-390e-e063-6294a90a2ed8 | 2026-07-02 | Warnings, Adverse reactions | 198051 KG60484QX9 |
| Omeprazole | OMEPRAZOLE | Unit Dose Solutions, Inc. | 557d4c2c-5541-3a51-e063-6394a90ad278 | 2026-06-30 | Warnings, Adverse reactions | 198051 KG60484QX9 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.