NDC 70710-1832-01 - Diclofenac Potassium
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
- 70710-1832
- Requested NDC
- 70710-1832-01
- Package NDCs from labels
- 70710-1832-1, 70710-1832-5, 70710-1832-0, 70710-1832-01
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2026-04-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diclofenac Potassium Tablets - Bryant Ranch Prepack | Bryant Ranch Prepack | 2026-04-09 | HUMAN PRESCRIPTION DRUG LABEL |
| Diclofenac Potassium Tablets - Zydus Pharmaceuticals (USA) Inc. | UMEDICA LABORATORIES PRIVATE LIMITED | Zydus Pharmaceuticals (USA) Inc. | UMEDICA LABORATORIES PRIVATE LIMITED | 2026-01-08 | HUMAN PRESCRIPTION DRUG LABEL |
| Diclofenac Potassium Tablets - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2025-02-05 | HUMAN PRESCRIPTION DRUG LABEL |
| Diclofenac Potassium Tablets - A-S Medication Solutions | A-S Medication Solutions | 2023-10-26 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1832-0 | Diclofenac Potassium | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | 8 | |
| 70710-1832-1 | Diclofenac Potassium | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 8 | |
| 70710-1832-5 | Diclofenac Potassium | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1832 | DICLOFENAC POTASSIUM (DICLOFENAC POTASSIUM TABLETS) TABLET, FILM COATED [ZYDUS PHARMACEUTICALS (USA) INC.] | 7 | Current NDC, Legacy NDC, 3 package rows | 20241225_1aa3d8d6-dd1c-46c7-96f9-2b5c9d72764a.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70710-1832-1 | EA - Each | 70710-1832 | 028b95fb-84ce-4ac1-8014-a462ad75c502 | 1 | 2022-07-06 |
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 |
|---|---|---|---|---|---|---|
| TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted) | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDE | Allergan, Inc. | 6a996e03-907f-4e6a-b232-0892b86956b0 | 2015-08-21 | Warnings | 15FIX9V2JP |
| Renewal Firming Day Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | BURT'S BEES, INC. | 18ceb5d8-4b76-6a54-e054-00144ff88e88 | 2015-06-18 | Warnings | 15FIX9V2JP |
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD. | 30468afc-9616-4765-b046-12e97a0a7827 | 2010-12-20 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.