NDC 72162-1734-00 - Diclofenac Sodium Delayed Release
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
- 72162-1734
- Requested NDC
- 72162-1734-00
- Package NDCs from labels
- 72162-1734-0, 72162-1734-5, 72162-1734-1, 72162-1734-9, 72162-1734-6, 72162-1734-3, 72162-1734-4, 72162-1734-8, 72162-1734-7, 72162-1734-00
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2024-02-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diclofenac Sodium Delayed Release - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-02-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72162-1734-0 | Diclofenac Sodium Delayed Release | 1000 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 1000 | 103 | |
| 72162-1734-1 | Diclofenac Sodium Delayed Release | 100 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 100 | 103 | |
| 72162-1734-3 | Diclofenac Sodium Delayed Release | 30 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 30 | 103 | |
| 72162-1734-4 | Diclofenac Sodium Delayed Release | 20 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 20 | 103 | |
| 72162-1734-5 | Diclofenac Sodium Delayed Release | 500 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 500 | 103 | |
| 72162-1734-6 | Diclofenac Sodium Delayed Release | 60 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 60 | 103 | |
| 72162-1734-7 | Diclofenac Sodium Delayed Release | 14 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 14 | 103 | |
| 72162-1734-8 | Diclofenac Sodium Delayed Release | 15 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 15 | 103 | |
| 72162-1734-9 | Diclofenac Sodium Delayed Release | 90 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 90 | 103 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72162-1734 | DICLOFENAC SODIUM DELAYED RELEASE (DICLOFENAC SODIUM) TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK] | 103 | Current NDC, 9 package rows | 20250215_df5bb0e7-a3a9-4650-aae7-9a11ce615d5d.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72162-1734-1 | EA - Each | 72162-1734 | 746f107c-f75a-4654-bb17-1bb3d73af14a | 1 | 2023-12-05 |
| 72162-1734-3 | EA - Each | 72162-1734 | 46b75da2-7ea6-49ae-96a3-2771ac5261c1 | 1 | 2023-10-16 |
| 72162-1734-4 | EA - Each | 72162-1734 | 9d64d354-5822-4c53-a1cd-038373ce53f2 | 1 | 2023-10-16 |
| 72162-1734-6 | EA - Each | 72162-1734 | 4375e3db-d2d9-4e87-bbe4-fad560b57c7c | 1 | 2023-10-16 |
| 72162-1734-7 | EA - Each | 72162-1734 | b76fb1ec-63d9-4fc1-adc1-b1b5a74775bf | 1 | 2023-10-16 |
| 72162-1734-8 | EA - Each | 72162-1734 | 8cc6b915-6ac8-4b8a-b18e-786f564ba1d6 | 1 | 2023-10-16 |
| 72162-1734-9 | EA - Each | 72162-1734 | bc394c15-2ec6-4da5-889f-d126deff26b5 | 1 | 2023-10-16 |
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 |
|---|---|---|---|---|---|---|
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | W Aesthetics | 5b0f2c8f-d6fa-5e25-e063-6394a90a084d | 2026-09-09 | Warnings | 15FIX9V2JP |
| Leader Artificial Tears 15 mL | POLYVINYL ALCOHOL, POVIDONE | Cardinal Health | 8cccc589-3a8e-baad-e053-2a95a90ab8c7 | 2026-09-09 | Warnings | FZ989GH94E |
| FRESHKOTE PRESERVATIVE FREE LUBRICANT EYE DROPS | POVIDONE, POLYVINYL ALCOHOL SOLUTION | Harrow Eye, LLC | 049e9cc9-0663-53bc-e063-6294a90a2c4f | 2026-09-04 | Warnings | FZ989GH94E |
| 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 |
| MZANK SUNSCREEN DAILY ULTIMATE PROTECTION SPF50 | SUNSCREEN SPF50 | Guangzhou Meixi Biotechnology Co., Ltd. | 5a0b4bd2-f6ad-35dc-e063-6294a90a8a66 | 2026-08-27 | Warnings | 15FIX9V2JP |
| MELAO Hydrating Lightweight Sunscreen | AVOBENZONE,ENSULIZOLE,HOMOSALATE,OCTISALATE,OCTOCRYLENE,TITANIUM DIOXIDE | Guangdong Aimu Biological Technology Co., Ltd | 59eeaea1-d726-99f3-e063-6394a90aeea3 | 2026-08-26 | Warnings | 15FIX9V2JP |
| Q Skin Science | SUNSCREEN | International Cosmeceuticals, Inc | 59e4c3d0-ee4c-2350-e063-6394a90ac9d2 | 2026-08-25 | Warnings | 15FIX9V2JP |
| MELAO zinc stick(GREEN) | TITANIUM DIOXIDE,ZINC OXIDE,OCTOCRYLENE | Guangzhou Haishi Biological Technology Co., Ltd. | 59c70c82-f7ff-9a04-e063-6294a90a7b3d | 2026-08-24 | Warnings | 15FIX9V2JP |
| SKIN-INFUSED FOUNDATION SPF 25/ Mineral sunscreen broad Spectrum SPF 25 01 | ZINC OXIDE, TITANIUM DIOXIDE | Cosmuses Cosmetics (Ningbo) Co., Ltd. | 59d74e3f-e3fa-a7a9-e063-6294a90a76e5 | 2026-08-24 | Warnings | 15FIX9V2JP |
| DICLOFENAC SODIUM | DICLOFENAC SODIUM | Northwind Health Company, LLC | 5990259d-2f90-20d3-e063-6394a90a3d23 | 2026-08-21 | Boxed warning, Warnings, Adverse reactions | 855926 QTG126297Q |
| Rohto Optic Glow | NAPHAZOLINE HYDROCHLORIDE, POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | df9c5f7c-96e6-4b2b-b8cb-21a6a3342dff | 2026-08-20 | Warnings | FZ989GH94E |
| Rohto All-In-One | HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE | The Mentholatum Company | 43e690e4-b381-46e3-838c-33aef5bdadde | 2026-08-20 | Warnings | 3NXW29V3WO |
| Sweat Resistant Sunscreen Body Original | TITANIUM DIOXIDE, ZINC OXIDE | Clutch, Inc. | 4bbde755-e312-123e-e063-6294a90a467f | 2026-08-20 | Warnings | 15FIX9V2JP |
| 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 |
| Rohto Preservative Free Dry Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | f4b1974c-2412-45f6-b79d-88b8a0bcb608 | 2026-08-18 | Warnings | FZ989GH94E |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.