NDC 65862-600-06 - RIZATRIPTAN BENZOATE
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
- 65862-600
- Requested NDC
- 65862-600-06
- Package NDCs from labels
- 65862-600-03, 65862-600-90, 65862-600-12, 65862-600-06, 65862-600-18
- Manufacturer
- DIRECT RX
- Effective date
- 2026-03-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| RIZATRIPTAN BENZOATE - DIRECT RX | DIRECT RX | 2026-03-17 | HUMAN PRESCRIPTION DRUG LABEL |
| Rizatriptan Benzoate - Aurobindo Pharma Limited | Aurobindo Pharma Limited | 2024-02-17 | Human Prescription Drug Label |
| Rizatriptan Benzoate - Proficient Rx LP | Proficient Rx LP | 2022-05-01 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 65862-600-03 | Rizatriptan Benzoate | 3 in 1 BLISTER PACK | TABLET | 3 | 14 | |
| 65862-600-06 | Rizatriptan Benzoate | 6 in 1 BLISTER PACK | TABLET | 6 | 14 | |
| 65862-600-12 | Rizatriptan Benzoate | 4 in 1 CARTON | TABLET | 4 | 14 | |
| 65862-600-18 | Rizatriptan Benzoate | 3 in 1 CARTON | TABLET | 3 | 14 | |
| 65862-600-90 | Rizatriptan Benzoate | 3 in 1 CARTON | TABLET | 3 | 14 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 65862-600-03 | EA - Each | 65862-600 | 7ea2a346-4cdc-463c-a0bb-a392009716ad | 1 | 2013-02-13 |
| 65862-600-12 | EA - Each | 65862-600 | 56ce3e0e-3e92-4136-8ee7-a9899a6ac6f1 | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| RIZATRIPTAN BENZOATE | ACTIVE INGREDIENT | WR978S7QHH | RIZATRIPTAN BENZOATE TABLET [AUROBINDO PHARMA LIMITED] | 3 | |
| RIZATRIPTAN | ACTIVE MOIETY | 51086HBW8G | RIZATRIPTAN BENZOATE TABLET [AUROBINDO PHARMA LIMITED] | 3 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | RIZATRIPTAN BENZOATE TABLET [AUROBINDO PHARMA LIMITED] | 3 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | RIZATRIPTAN BENZOATE TABLET [AUROBINDO PHARMA LIMITED] | 3 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | RIZATRIPTAN BENZOATE TABLET [AUROBINDO PHARMA LIMITED] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | RIZATRIPTAN BENZOATE TABLET [AUROBINDO PHARMA LIMITED] | 3 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | RIZATRIPTAN BENZOATE TABLET [AUROBINDO PHARMA LIMITED] | 3 |
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 |
|---|---|---|---|---|---|---|
| Mold, Yeast and Dust | ACREMONIUM STRICTUM, ADRENALINUM, ALLIUM CEPA, ALTERNARIA ALTERNATA, ARSENICUM IODATUM, ASPERGILLUS FUMIGATUS, ASPERGILLUS NIGER, AUREOBASIDIUM PULLULANS, CANDIDA ALBICANS, CLADOSPORIUM HERBARUM, COCKROACH, DERMATOPHAGOIDES FARINAE, EPICOCCUM PURPURASCENS, FUSARIUM SOLANI, HISTAMINUM HYDROCHLORICUM, LYCOPODIUM CLAVATUM, MUCOR CIRCINELLOIDES, NATRUM SULPHURICUM, RHIZOPUS STOLONIFER, SACCHAROMYCES CEREVISIAE, SILICEA | NaturalCare | e0f53f47-acd9-43e2-a7a2-2a500bc9dc1b | 2026-02-03 | Warnings | ETJ7Z6XBU4 |
| Aquavit 1 | AQUAVIT 1 | Uriel Pharmacy Inc. | 2354fcfc-05a2-444a-ace4-b3df61413157 | 2026-02-02 | Warnings | 1K09F3G675 |
| MAXALT | RIZATRIPTAN BENZOATE | Organon LLC | 007b4644-e0e7-4863-9ae3-fe09676b3f5f | 2026-01-29 | Warnings, Adverse reactions | 314209 WR978S7QHH |
| Calamine | CALAMINE | AMERISOURCE BERGEN | 90d9d908-57ea-4062-ade0-8a4888939c91 | 2026-01-29 | Warnings, Adverse reactions | 1K09F3G675 |
| BioMicroneedle PDRN Cream | SILICON DIOXIDE | Guangzhou Shengyanghui Industrial Trading Co., Ltd | 48e2edae-94ea-c42e-e063-6394a90a907b | 2026-01-21 | Warnings | ETJ7Z6XBU4 |
| Inflammation I | ECHINACEA (ANGUSTIFOLIA), NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, APIS MELLIFICA, BELLADONNA, FERRUM PHOSPHORICUM, NITRICUM ACIDUM, OLEANDER, SILICEA | BioActive Nutritional, Inc. | 3cb12181-ae7e-45c7-a1b1-e1952f36f8c3 | 2026-01-21 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | ATOSAFE CO., Ltd | 487c5036-0eb0-ada9-e063-6394a90aa02e | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | DONG IL PHARMS CO.,LTD | 487cd5b9-28f3-392d-e063-6394a90a9ba1 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE COOL MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | ATOSAFE CO., Ltd | 487cf27a-d761-6353-e063-6394a90af029 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | ATOSAFE CO., Ltd | 487d52d1-8853-bc90-e063-6394a90ab91d | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE COOL MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | DONG IL PHARMS CO.,LTD | 487d689d-ebdd-43c3-e063-6294a90af0e2 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | DONG IL PHARMS CO.,LTD | 487da363-1d01-8cdc-e063-6294a90ac24d | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| Lotrimin Daily Sweat and Odor Control | TOPICAL STARCH | Bayer HealthCare LLC. | 9ec5c80d-b550-496f-e053-2a95a90a5489 | 2026-01-16 | Warnings | O8232NY3SJ |
| Berberis Quartz | BERBERIS QUARTZ | Uriel Pharmacy Inc. | 5da48d70-1140-495d-b672-0e55c04196e1 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| Constipation Relief | ALUMINUM OXIDE, BRYONIA ALBA ROOT, SODIUM CHLORIDE, GRAPHITE, SILICON DIOXIDE | Homeocare Laboratories | 62374240-cd14-44e2-9405-5f8996faf047 | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| Menopause Relief | BARIUM CARBONATE, ATROPA BELLADONNA, BLACK COHOSH, NITROGLYCERIN, LACHESIS MUTA VENOM, SILICON DIOXIDE | Homeocare Laboratories | 99b182d5-4102-4b25-85d3-f4be077d753f | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| Amber Amethyst | AMBER AMETHYST | Uriel Pharmacy, Inc | 4837e805-a777-c1fa-e063-6294a90ae9c4 | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| ECHINACEA | ECHINACEA ANGUSTIFOLIA, HAMAMMELIS VIRGINIANA, CALCAREA PHOSPHORICA, HYDRASTIS CANADANESIS, SENEGA OFFICINALIS, SILICEA, CONIUM, AURUM MURIATICUM NATRONATUM, CALCAREA CARBONICA, FUCUS VESICULOSUS, LACHESIS MUTUS | Marco Pharma International LLC. | 7efadb70-99e4-428b-a8ef-a2797327c6fa | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| RET Stomach 7001 | RET STOMACH | Professional Complementary Health Formulas | 086427e0-599e-4405-a996-d949023f9d90 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Organophosphate Combination 9309 | ORGANOPHOSPHATE COMBINATION | Professional Complementary Health Formulas | f777015f-1df6-4821-af63-543175313aba | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.