NDC 80425-0189-03 - Diclofenac Sodium 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
- 80425-0189
- Requested NDC
- 80425-0189-03
- Package NDCs from labels
- 80425-0189-1, 80425-0189-2, 80425-0189-3, 80425-0189-03
- Manufacturer
- Advanced Rx Pharmacy 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 |
|---|---|---|---|
| Diclofenac Sodium DR - Advanced Rx Pharmacy of Tennessee, LLC | Advanced Rx Pharmacy of Tennessee, LLC | 2024-12-31 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80425-0189-1 | Diclofenac SodiumDR | 60 in 1 BOTTLE | TABLET, DELAYED RELEASE | 60 | 6 | |
| 80425-0189-2 | Diclofenac SodiumDR | 30 in 1 BOTTLE | TABLET, DELAYED RELEASE | 30 | 6 | |
| 80425-0189-3 | Diclofenac SodiumDR | 90 in 1 BOTTLE | TABLET, DELAYED RELEASE | 90 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 80425-0189 | DICLOFENAC SODIUM DR (DICLOFENAC SODIUM) TABLET, DELAYED RELEASE [ADVANCED RX PHARMACY OF TENNESSEE, LLC] | 6 | Current NDC, Legacy NDC, 3 package rows | 20250101_d424ab84-2aaa-38a9-e053-2a95a90adde9.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 80425-0189-1 | EA - Each | 80425-0189 | 1cc1ed3c-bfe6-449b-8220-36962f0168af | 1 | 2023-03-13 |
| 80425-0189-2 | EA - Each | 80425-0189 | b2b4c1f7-3353-4bcb-947e-56e9782f23ed | 1 | 2023-04-07 |
| 80425-0189-3 | EA - Each | 80425-0189 | 0d40ec80-d802-40a2-b8c1-d0f7c388ca59 | 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 |
|---|---|---|---|---|---|---|
| Diclofenac Sodium | DICLOFENAC SODIUM | A-S Medication Solutions | d9698809-4887-4514-aa28-0066355ef908 | 2026-09-02 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| DICLOFENAC SODIUM | DICLOFENAC SODIUM | NuCare Pharmaceuticals, Inc. | 5a852412-69af-6502-e063-6294a90a0748 | 2026-09-02 | Boxed warning, Warnings, Adverse reactions | 855906 QTG126297Q |
| Diclofenac | DICLOFENAC SODIUM | YYBA CORP | 533653e8-93d5-9080-e063-6394a90a165b | 2026-09-01 | Warnings | QTG126297Q |
| Diclofenac sodium and Misoprostol | DICLOFENAC SODIUM AND MISOPROSTOL | Mylan Pharmaceuticals Inc. | a7701e8c-4e16-4165-8b83-de2c08d5ded3 | 2026-08-31 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| Diclofenac Sodium and Misoprostol | DICLOFENAC SODIUM AND MISOPROSTOL | Actavis Pharma, Inc. | df8b8660-0c24-4848-8bea-c1b935090c66 | 2026-08-31 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| DICLOFENAC SODIUM | DICLOFENAC SODIUM | Northwind Health Company, LLC | 5990259d-2f90-20d3-e063-6394a90a3d23 | 2026-08-21 | Boxed warning, Warnings, Adverse reactions | 855926 QTG126297Q |
| AMAZON BASIC CARE ARTHRITIS PAIN | DICLOFENAC SODIUM | Amazon.com Services LLC | 113e2f87-c408-3e44-e063-6394a90a0a7f | 2026-08-20 | Warnings | QTG126297Q |
| DICLOFENAC SODIUM | DICLOFENAC SODIUM | Northwind Health Company, LLC | 4dde6e36-7540-1cc3-e063-6294a90a3941 | 2026-08-19 | Boxed warning, Warnings, Adverse reactions | 855906 QTG126297Q |
| Diclofenac Sodium | DICLOFENAC SODIUM | Sportpharm LLC | e9ec5462-939a-4022-8946-5d81869a6277 | 2026-08-17 | Boxed warning, Warnings, Adverse reactions | 855926 QTG126297Q |
| Diclofenac sodium | DICLOFENAC SODIUM | EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC) | 2a7019e9-e20f-4897-9b8e-942a7f2b34f6 | 2026-08-12 | Warnings | QTG126297Q |
| Diclofenac Sodium | DICLOFENAC SODIUM | Preferred Pharmaceuticals Inc. | 226da8a2-807d-4784-8d33-b434f3951a52 | 2026-08-12 | Warnings | QTG126297Q |
| Diclofenac Sodium | DICLOFENAC SODIUM | PD-Rx Pharmaceuticals, Inc. | 681b6b25-4a28-44f2-8042-d5e01a502116 | 2026-08-12 | Boxed warning, Warnings, Adverse reactions | 855926 QTG126297Q |
| Diclofenac sodium | DICLOFENAC SODIUM | NuCare Pharmaceuticals, Inc. | 57c83158-f072-6fa2-e063-6394a90aee2c | 2026-07-29 | Warnings | QTG126297Q |
| Diclofenac Sodium Delayed Release | DICLOFENAC SODIUM | REMEDYREPACK INC. | ddd2278b-70be-41ca-8a84-e3fe0f1a1561 | 2026-07-28 | Boxed warning, Warnings, Adverse reactions | ANDA075185 855906 QTG126297Q |
| Diclofenac sodium | DICLOFENAC SODIUM | CVS Pharmacy | 591cc2ed-e667-4779-a426-8a2e6f873573 | 2026-07-22 | Warnings | QTG126297Q |
| DICLOFENAC SODIUM | DICLOFENAC SODIUM | Aurobindo Pharma Limited | d9b6f1d0-1710-46fb-8ea4-80b3ca60a575 | 2026-07-17 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| DICLOFENAC SODIUM | DICLOFENAC SODIUM | HAWAII REPACK, INC | ea113a58-c7ed-4768-9777-93d9b166dfbe | 2026-07-12 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| Diclofenac Sodium | DICLOFENAC SODIUM 1% | Sportpharm LLC | 391d9d0b-74b7-4359-aea0-d3bb8c8d3cd1 | 2026-07-10 | Warnings | QTG126297Q |
| Diclofenac Sodium | DICLOFENAC SODIUM | American Health Packaging | 63c00b50-06d3-4659-81cf-be4516429e81 | 2026-07-10 | Boxed warning, Warnings, Adverse reactions | 855906 QTG126297Q |
| DICLOFENAC SODIUM | DICLOFENAC SODIUM | REMEDYREPACK INC. | 6e6a6f98-5517-4f67-9a6a-71019ba2d773 | 2026-07-09 | Boxed warning, Warnings, Adverse reactions | 855906 QTG126297Q |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.