NDC 51672-4033-03 - Warfarin Sodium
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
- 51672-4033
- Requested NDC
- 51672-4033-03
- Package NDCs from labels
- 51672-4033-1, 51672-4033-3, 51672-4033-7, 51672-4033-0, 51672-4033-03
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd.
- Effective date
- 2025-06-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Warfarin Sodium | Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd. | 2025-06-10 | HUMAN PRESCRIPTION DRUG LABEL |
| Warfarin Sodium - Med-Health Pharma, LLC | Med-Health Pharma, LLC | 2012-01-20 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-4033-0 | Warfarin Sodium | 10 in 1 BLISTER PACK | TABLET | 10 | 14 | |
| 51672-4033-0 | Warfarin Sodium | 10 in 1 CARTON | TABLET | 10 | 14 | |
| 51672-4033-1 | Warfarin Sodium | 100 in 1 BOTTLE | TABLET | 100 | 14 | |
| 51672-4033-3 | Warfarin Sodium | 1000 in 1 BOTTLE | TABLET | 1000 | 14 | |
| 51672-4033-7 | Warfarin Sodium | 5000 in 1 BOTTLE | TABLET | 5000 | 14 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-4033 | WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.] | 13 | Current NDC, Legacy NDC, 5 package rows | 20231222_8ad881e0-ca41-42ad-9d7d-eb85b3a30af0.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-4033-1 | EA - Each | 51672-4033 | 961cae87-3df2-47c4-9726-49436f1de469 | 1 | 2012-07-24 |
| 51672-4033-3 | EA - Each | 51672-4033 | 46e78dcb-7244-4f3e-be03-0dc10ac852a6 | 1 | 2012-07-24 |
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 |
|---|---|---|---|---|---|---|
| Alumina | ALUMINUM OXIDE | Boiron | 84266aa8-b80c-a2a5-e053-2991aa0a68e0 | 2023-10-18 | LMI26O6933 | |
| Alumina | ALUMINUM OXIDE | Boiron | 8426b2bb-4401-9015-e053-2991aa0a0993 | 2023-10-18 | LMI26O6933 | |
| Alumina | ALUMINUM OXIDE | Boiron | 8426e977-2b24-fdf4-e053-2a91aa0a7c39 | 2023-10-18 | LMI26O6933 | |
| Alumina | ALUMINUM OXIDE | Boiron | 84b528ab-23f7-e42c-e053-2991aa0acc4d | 2023-10-18 | LMI26O6933 | |
| Anubis Barcelona | GLYCERIN, SORBITOL, ALOE BARBADENSIS LEAF JUICE | ANUBIS COSMETICS SL | eb651769-4d98-2b3b-e053-2a95a90a36b0 | 2023-09-01 | Warnings | H3R47K3TBD |
| Anubis Barcelona Total Hydrating | BETAINE, GLYCERIN, POLYSORBATE 20 | ANUBIS COSMETICS SL | eaefe3b9-9064-18b1-e053-2a95a90a5765 | 2023-09-01 | Warnings | H3R47K3TBD |
| Anubis Barcelona New Even | LACTIC ACID, CITRIC ACID, GLYCOLIC ACID | ANUBIS COSMETICS SL | eaeeb6e0-5322-20c4-e053-2995a90a9fd9 | 2023-09-01 | Warnings | H3R47K3TBD |
| Warfarin Sodium | WARFARIN SODIUM | A-S Medication Solutions | 35bf53df-994b-4c32-8bdb-9227e8e195c6 | 2023-08-30 | Boxed warning, Warnings, Adverse reactions | 855332 6153CWM0CL |
| Alumina | ALUMINUM OXIDE | Boiron | 84b4fd05-f2cc-3b45-e053-2991aa0ad5d9 | 2023-07-11 | LMI26O6933 | |
| Alumina | ALUMINA | Hahnemann Laboratories, INC. | ffdbdb70-8666-f0c6-e053-6394a90a6596 | 2023-07-06 | LMI26O6933 | |
| Alumina | ALUMINUM OXIDE | Boiron | a9603cb0-7c3b-11e6-8197-424c58303031 | 2023-06-26 | LMI26O6933 | |
| Warfarin Sodium | WARFARIN | Bryant Ranch Prepack | c41b7c23-8053-428a-ac1d-8395e714c2f1 | 2023-04-12 | Boxed warning, Warnings, Adverse reactions | 855318 6153CWM0CL |
| Alumina | ALUMINUM OXIDE | Boiron | 8426bd35-372c-4417-e053-2a91aa0a7903 | 2023-04-11 | LMI26O6933 | |
| Alumina | ALUMINUM OXIDE | Boiron | 84274737-2fed-d542-e053-2a91aa0a1ead | 2023-03-28 | LMI26O6933 | |
| Alumina | ALUMINUM OXIDE | Boiron | 84270ebe-2cd9-7fb5-e053-2a91aa0ab7d5 | 2023-03-27 | LMI26O6933 | |
| COLIC CP | AETHUSA CYNAPIUM, ALUMINUM OXIDE, BRYONIA ALBA ROOT, OYSTER SHELL CALCIUM CARBONATE CRUDE, MATRICARIA RECUTITA, LYCOPODIUM CLAVATUM SPORE, PHOSPHORUS, ANEMONE PULSATILLA, SILICON DIOXIDE, SULFUR. | Natural Creations, Inc. | 7c2a2f6e-a332-4c68-a7a8-fdc390f1827e | 2022-12-19 | Warnings | LMI26O6933 |
| Metals Detox | ALUMINA, ARSENICUM METALLICUM, MERCURIUS CORROSIVUS, NICCOLUM METALLICUM, PLUMBUM METALLICUM, RADIUM BROMATUM, STANNUM METALLICUM | ProBLEN | 41b750f2-7330-4769-aa48-4ec3537116c1 | 2022-11-30 | Warnings | LMI26O6933 |
| Warfarin Sodium | WARFARIN SODIUM | Proficient Rx LP | 388bfa49-f4f7-412a-80ff-d09442489e2b | 2022-04-01 | Boxed warning, Warnings, Adverse reactions | 855332 6153CWM0CL |
| CONSTIPATION CP | ALUMINUM OXIDE, BRYONIA ALBA ROOT, MATRICARIA RECUTITA, GRAPHITE, LYCOPODIUM CLAVATUM SPORE, STRYCHNOS NUX-VOMICA SEED, SILICON DIOXIDE, SULFUR, SODIUM CHLORIDE, MAGNESIUM CHLORIDE, LEAD, SEPIA OFFICINALIS JUICE. | Natural Creations, Inc. | 961b3ddf-41fe-46ed-b5e4-0fd8d9652edf | 2021-11-15 | Warnings | LMI26O6933 |
| ALUMINA | ALUMINA | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc | f23b1f6d-d962-482b-9479-dcddf793aad3 | 2021-09-26 | Warnings | LMI26O6933 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.