NDC 0832-1214-89 - 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
- 0832-1214
- Requested NDC
- 0832-1214-89
- Package NDCs from labels
- 0832-1214-00, 0832-1214-10, 0832-1214-89, 0832-1214-01
- 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 |
|---|---|---|---|---|---|---|
| 0832-1214-00 | Jantoven | 100 in 1 BOTTLE | TABLET | 100 | 13 | |
| 0832-1214-01 | Jantoven | 100 in 1 CARTON | TABLET | 100 | 13 | |
| 0832-1214-10 | Jantoven | 1000 in 1 BOTTLE | TABLET | 1000 | 13 | |
| 0832-1214-89 | 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 |
|---|---|---|---|---|---|
| 0832-1214-00 | EA - Each | 0832-1214 | 13eaedfa-8802-46b2-aea0-951d839e4a1e | 1 | 2012-07-24 |
| 0832-1214-01 | EA - Each | 0832-1214 | e2bbd980-0575-4250-b161-a163b2a41a1d | 1 | 2012-07-24 |
| 0832-1214-10 | EA - Each | 0832-1214 | bf1cd59c-8485-4dcd-b804-a2d06a769327 | 1 | 2012-07-24 |
| 0832-1214-89 | EA - Each | 0832-1214 | fd906e71-9aa6-40f9-8a45-d6aa86e60c92 | 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 |
|---|---|---|---|---|---|---|
| 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 |
| Warfarin Sodium | WARFARIN | Coupler LLC | 5a5b5e3a-6556-a542-e063-6294a90a6d3f | 2026-08-31 | Boxed warning, Warnings, Adverse reactions | 855312 6153CWM0CL |
| Warfarin Sodium | WARFARIN SODIUM | Cardinal Health 107, LLC | 7c4deb97-9966-4c8e-9ba6-bb260b71e130 | 2026-08-25 | Boxed warning, Warnings, Adverse reactions | 855312 6153CWM0CL |
| Warfarin Sodium | WARFARIN | Coupler LLC | 598e5e2e-9264-8371-e063-6394a90aaf18 | 2026-08-21 | Boxed warning, Warnings, Adverse reactions | 855318 6153CWM0CL |
| Rohto Optic Glow | NAPHAZOLINE HYDROCHLORIDE, POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | df9c5f7c-96e6-4b2b-b8cb-21a6a3342dff | 2026-08-20 | Warnings | FZ989GH94E |
| Rohto Preservative Free Dry Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | f4b1974c-2412-45f6-b79d-88b8a0bcb608 | 2026-08-18 | Warnings | FZ989GH94E |
| Rohto Dry-Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | 8ea5c6c9-48f4-406a-a2cb-9280c546d87d | 2026-08-18 | Warnings | FZ989GH94E |
| Warfarin Sodium | WARFARIN SODIUM | REMEDYREPACK INC. | bd6ea120-5d1c-4815-94f2-81e28dc6b7a9 | 2026-08-10 | Boxed warning, Warnings, Adverse reactions | 855318 6153CWM0CL |
| GOOD NEIGHBOR PHARMACY ARTIFICAL TEARS LUBRICANT EYE DROPS | POLYVINYL ALCOHOL, POVIDONE | AmerisourceBergen | ce6852a8-c5e6-403d-a7b4-a2e85d1ebb1f | 2026-07-22 | Warnings | FZ989GH94E |
| Warfarin Sodium | WARFARIN SODIUM | REMEDYREPACK INC. | 724b0061-f42a-4008-a078-09c800ee9785 | 2026-07-01 | Boxed warning, Warnings, Adverse reactions | 855288 6153CWM0CL |
| Warfarin Sodium | WARFARIN | REMEDYREPACK INC. | d7fb4290-ed37-4ed3-ae51-c400191961dc | 2026-06-30 | Boxed warning, Warnings, Adverse reactions | 855338 6153CWM0CL |
| Warfarin Sodium | WARFARIN | REMEDYREPACK INC. | 51e98fb6-ba76-497e-95d8-fe895ef0b7ed | 2026-06-29 | Boxed warning, Warnings, Adverse reactions | 855312 6153CWM0CL |
| Warfarin Sodium | WARFARIN | REMEDYREPACK INC. | a4cf3107-5646-4b91-8aae-94548e4409ef | 2026-06-29 | Boxed warning, Warnings, Adverse reactions | 855288 6153CWM0CL |
| Warfarin Sodium | WARFARIN | REMEDYREPACK INC. | 2fb8b8d5-f643-4069-8e47-5eae31a8fbc8 | 2026-06-29 | Boxed warning, Warnings, Adverse reactions | 855344 6153CWM0CL |
| Warfarin Sodium | WARFARIN | REMEDYREPACK INC. | 884cdbf6-0a52-4126-8e14-b0d7c9367e33 | 2026-06-29 | Boxed warning, Warnings, Adverse reactions | 855318 6153CWM0CL |
| Warfarin Sodium | WARFARIN | REMEDYREPACK INC. | 8eddba53-19c4-411b-b0d4-cb2f948ba125 | 2026-06-29 | Boxed warning, Warnings, Adverse reactions | 855296 6153CWM0CL |
| Warfarin Sodium | WARFARIN | REMEDYREPACK INC. | 2cbcc99d-9107-4d39-a1e9-e19305de8b5d | 2026-06-25 | Boxed warning, Warnings, Adverse reactions | 855302 6153CWM0CL |
| Warfarin Sodium | WARFARIN | REMEDYREPACK INC. | 8ee94789-72d2-4c42-9dbd-0501e9767d97 | 2026-06-25 | Boxed warning, Warnings, Adverse reactions | 855332 6153CWM0CL |
| Warfarin Sodium | WARFARIN | REMEDYREPACK INC. | 545ec40d-2db1-4581-b3ec-ce195e5f5400 | 2026-06-25 | Boxed warning, Warnings, Adverse reactions | 855324 6153CWM0CL |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.