NDC 0832-1218-89 - Jantoven
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
- 0832-1218
- Requested NDC
- 0832-1218-89
- Package NDCs from labels
- 0832-1218-00, 0832-1218-50, 0832-1218-89, 0832-1218-01
- Manufacturer
- Upsher-Smith Laboratories, LLC | Bora Pharmaceuticals, Inc
- Effective date
- 2025-07-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Jantoven - Upsher-Smith Laboratories, LLC | Bora Pharmaceuticals, Inc | Upsher-Smith Laboratories, LLC | Bora Pharmaceuticals, Inc | 2025-07-08 | HUMAN PRESCRIPTION DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0832-1218-00 | Jantoven | 100 in 1 BOTTLE | TABLET | 100 | 13 | |
| 0832-1218-01 | Jantoven | 100 in 1 CARTON | TABLET | 100 | 13 | |
| 0832-1218-50 | Jantoven | 500 in 1 BOTTLE | TABLET | 500 | 13 | |
| 0832-1218-89 | Jantoven | 1 in 1 BLISTER PACK | TABLET | 1 | 13 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0832-1218-00 | EA - Each | 0832-1218 | 4f75a7af-c1b9-4c44-9d39-261c64b4890d | 1 | 2012-07-24 |
| 0832-1218-01 | EA - Each | 0832-1218 | dacef602-c55b-4cbe-be36-d51196c18958 | 1 | 2012-07-24 |
| 0832-1218-50 | EA - Each | 0832-1218 | 507f05c8-30f0-4fae-8571-4506e3cf8406 | 1 | 2012-07-24 |
| 0832-1218-89 | EA - Each | 0832-1218 | 2b818c29-8420-47b1-9e18-5fb7360515bd | 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 |
|---|---|---|---|---|---|---|
| Warfarin Sodium | WARFARIN SODIUM | REMEDYREPACK INC. | f5fb1a5f-0dda-4f47-8683-ea63ac88a69d | 2026-06-24 | Boxed warning, Warnings, Adverse reactions | 855332 6153CWM0CL |
| Warfarin Sodium | WARFARIN SODIUM | REMEDYREPACK INC. | 1244c338-9140-425a-bf2a-9da6b4ac0287 | 2026-06-24 | Boxed warning, Warnings, Adverse reactions | 855302 6153CWM0CL |
| Warfarin Sodium | WARFARIN SODIUM | REMEDYREPACK INC. | d6083d68-4360-4d47-a1b2-1eb2763024bb | 2026-06-24 | Boxed warning, Warnings, Adverse reactions | 855296 6153CWM0CL |
| Warfarin Sodium | WARFARIN SODIUM | REMEDYREPACK INC. | 4dc2d94e-f856-47da-9d44-24773d97eb87 | 2026-06-24 | Boxed warning, Warnings, Adverse reactions | 855318 6153CWM0CL |
| Warfarin Sodium | WARFARIN SODIUM | REMEDYREPACK INC. | ba65ae56-ca3b-4895-9938-1dde2c3d34bf | 2026-06-24 | Boxed warning, Warnings, Adverse reactions | 855324 6153CWM0CL |
| Warfarin Sodium | WARFARIN SODIUM | A-S Medication Solutions | 8cd0e744-b499-4344-b1db-59f85950e169 | 2026-06-22 | Boxed warning, Warnings, Adverse reactions | 855288 6153CWM0CL |
| Rohto Sun and Sport | HYPROMELLOSE, POVIDONE | The Mentholatum Company | 8bcc8882-b886-4b55-9bc4-d4b92a41358f | 2026-06-19 | Warnings | FZ989GH94E |
| Rohto Dual Light Relief | HYPROMELLOSE, POVIDONE | The Mentholatum Company | 1b597f83-d7f1-cf93-e063-6394a90a99f7 | 2026-06-19 | Warnings | FZ989GH94E |
| Warfarin Sodium | WARFARIN SODIUM | A-S Medication Solutions | 991b1e3e-236e-44cf-ad61-7233f777ce67 | 2026-06-15 | Boxed warning, Warnings, Adverse reactions | 855302 6153CWM0CL |
| Warfarin Sodium | WARFARIN | Amneal Pharmaceuticals LLC | 558b7a0d-5490-4c1b-802e-3ab3f1efe760 | 2026-05-29 | Boxed warning, Warnings, Adverse reactions | 855324 855296 855344 855302 855288 855338 855318 855312 855332 6153CWM0CL |
| Warfarin Sodium | WARFARIN | Coupler LLC | 52bacf1e-9ba8-7eca-e063-6394a90ab60b | 2026-05-26 | Boxed warning, Warnings, Adverse reactions | 855288 6153CWM0CL |
| Ripple | GLYCERIN, POVIDONE | CorneaCare Inc | 3b5ba197-d501-681e-e063-6294a90aefb5 | 2026-05-24 | Warnings | FZ989GH94E |
| Warfarin Sodium | WARFARIN | Coupler LLC | 5256c518-31bf-f73b-e063-6394a90a71da | 2026-05-21 | Boxed warning, Warnings, Adverse reactions | 855302 6153CWM0CL |
| iVIZIA Lubricant Eye Gel | POVIDONE | Thea Pharma Inc. | 1f06ca1a-5270-9a82-e063-6294a90aed64 | 2026-04-29 | Warnings | FZ989GH94E |
| GoodSense Eye Drops Advanced Relief Moisturizer | DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL | Preferred PHarmaceuticals Inc. | 011473a8-26d5-4661-b3c0-745f9b6aa1d8 | 2026-04-29 | Warnings | FZ989GH94E |
| Warfarin Sodium | WARFARIN SODIUM | REMEDYREPACK INC. | 6b227c9e-02e9-4ec9-8b11-3ab6fe5093e5 | 2026-04-27 | Boxed warning, Warnings, Adverse reactions | 855312 6153CWM0CL |
| Warfarin Sodium | WARFARIN SODIUM | REMEDYREPACK INC. | 72d3ea20-27e4-4368-a666-a9b76530dbb9 | 2026-04-27 | Boxed warning, Warnings, Adverse reactions | 855332 6153CWM0CL |
| Warfarin Sodium | WARFARIN SODIUM | REMEDYREPACK INC. | 61ab23a7-bc67-4777-854a-bf43c788a69a | 2026-04-27 | Boxed warning, Warnings, Adverse reactions | 855344 6153CWM0CL |
| Warfarin Sodium | WARFARIN SODIUM | REMEDYREPACK INC. | 7b3b6f89-1feb-4939-a95b-7ad0707f4d76 | 2026-04-27 | Boxed warning, Warnings, Adverse reactions | 855296 6153CWM0CL |
| Warfarin Sodium | WARFARIN SODIUM | REMEDYREPACK INC. | 73b8e5ab-86f8-44f8-b290-346acb81c9ae | 2026-04-27 | Boxed warning, Warnings, Adverse reactions | 855288 6153CWM0CL |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.