NDC 68084-735-11 - Fluconazole
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
- 68084-735
- Requested NDC
- 68084-735-11
- Package NDCs from labels
- 68084-735-11, 68084-735-01
- Manufacturer
- American Health Packaging
- Effective date
- 2025-07-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Fluconazole - American Health Packaging | American Health Packaging | 2025-07-23 | HUMAN PRESCRIPTION DRUG LABEL |
| Fluconazole - Cardinal Health | Cardinal Health | 2020-07-02 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68084-735-01 | Fluconazole | 100 in 1 BOX, UNIT-DOSE | TABLET | 100 | 12 | |
| 68084-735-11 | Fluconazole | 1 in 1 BLISTER PACK | TABLET | 1 | 12 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68084-735-01 | EA - Each | 68084-735 | 657e3eb7-d9f2-42c4-8dc6-325161bef759 | 1 | 2014-10-03 |
| 68084-735-11 | EA - Each | 68084-735 | 7460fb53-704c-4063-87b5-8f2278b765e5 | 1 | 2014-10-03 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| FLUCONAZOLE | ACTIVE INGREDIENT | 8VZV102JFY | FLUCONAZOLE TABLET [AMERICAN HEALTH PACKAGING] | 3 | |
| FLUCONAZOLE | ACTIVE MOIETY | 8VZV102JFY | FLUCONAZOLE TABLET [AMERICAN HEALTH PACKAGING] | 3 | |
| CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS | INACTIVE INGREDIENT | L11K75P92J | FLUCONAZOLE TABLET [AMERICAN HEALTH PACKAGING] | 3 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | FLUCONAZOLE TABLET [AMERICAN HEALTH PACKAGING] | 3 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | FLUCONAZOLE TABLET [AMERICAN HEALTH PACKAGING] | 3 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | FLUCONAZOLE TABLET [AMERICAN HEALTH PACKAGING] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | FLUCONAZOLE TABLET [AMERICAN HEALTH PACKAGING] | 3 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | FLUCONAZOLE TABLET [AMERICAN HEALTH PACKAGING] | 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 |
|---|---|---|---|---|---|---|
| Fluconazole | FLUCONAZOLE | Northwind Health Company, LLC | 0de7211d-b8ce-214d-e063-6294a90aec41 | 2026-06-22 | Warnings, Adverse reactions | 197699 8VZV102JFY |
| 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 |
| Fluconazole | FLUCONAZOLE | REMEDYREPACK INC. | 726daf35-4c03-464f-a814-cc0a715d6031 | 2026-06-12 | Warnings, Adverse reactions | ANDA077731 197700 8VZV102JFY |
| Fluconazole | FLUCONAZOLE | PD-Rx Pharmaceuticals, Inc. | dd975843-c3e4-44f4-bb0d-33b294c1f6fb | 2026-06-12 | Warnings, Adverse reactions | 197700 8VZV102JFY |
| Fluconazole | FLUCONAZOLE | REMEDYREPACK INC. | 91adb548-9875-47e9-8054-578ed8c7572e | 2026-06-10 | Warnings, Adverse reactions | 197698 8VZV102JFY |
| Ripple | GLYCERIN, POVIDONE | CorneaCare Inc | 3b5ba197-d501-681e-e063-6294a90aefb5 | 2026-05-24 | Warnings | FZ989GH94E |
| Fluconazole | FLUCONAZOLE | ASCLEMED USA INC. | 2099c3a0-1911-4d4a-878a-36cf054bdd0b | 2026-05-20 | Warnings, Adverse reactions | ANDA077731 197698 197699 197700 197701 8VZV102JFY |
| Fluconazole | FLUCONAZOLE | Bryant Ranch Prepack | e222031d-58f6-46d6-99f8-320b9aacf2b2 | 2026-05-18 | Warnings, Adverse reactions | 197699 8VZV102JFY |
| Fluconazole | FLUCONAZOLE | Coupler LLC | 519e44f4-9318-572e-e063-6394a90afe93 | 2026-05-12 | Warnings, Adverse reactions | 197698 8VZV102JFY |
| Fluconazole | FLUCONAZOLE | REMEDYREPACK INC. | 2cbf3c6c-318c-4dd9-ad44-a8eb9eccb0f5 | 2026-05-01 | Warnings, Adverse reactions | 197699 8VZV102JFY |
| 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 |
| Fluconazole | FLUCONAZOLE | Cardinal Health 107, LLC | f1bfba3a-5b18-41c0-9084-b1f26bb93ef2 | 2026-04-27 | Warnings, Adverse reactions | 197698 197700 8VZV102JFY |
| Fluconazole | FLUCONAZOLE | Sportpharm LLC | 8a4d6d9e-02ae-42e4-83ec-f5c4e135273b | 2026-04-24 | Warnings, Adverse reactions | 197698 197699 197700 197701 8VZV102JFY |
| Fluconazole | FLUCONAZOLE | Preferred Pharmaceuticals Inc. | eeeb82e1-d668-418e-9716-f8bcf72f80c0 | 2026-04-17 | Warnings, Adverse reactions | ANDA077731 197700 8VZV102JFY |
| Fluconazole | FLUCONAZOLE | Preferred Pharmaceuticals Inc. | 5cbd78cd-2cd7-4882-9902-bdb7812fbc6b | 2026-04-16 | Warnings, Adverse reactions | ANDA077731 197699 8VZV102JFY |
| FreshKote Preservative Free Lubricant Eye Drops | POVIDONE, POLYVINYL ALCOHOL | Eyevance Pharmaceuticals | f51c50c3-43ae-4169-9d2b-22b239461dd1 | 2026-04-08 | Warnings | FZ989GH94E |
| fluconazole | FLUCONAZOLE | Zydus Pharmaceuticals (USA) Inc. | d1364455-1537-46d4-b093-38cca3be778f | 2026-04-07 | Warnings, Adverse reactions | 197698 197699 197700 197701 8VZV102JFY |
| Fluconazole | FLUCONAZOLE | Mylan Pharmaceuticals Inc. | 737e0fac-a2d2-4053-a0d7-edbfb6248f69 | 2026-04-02 | Warnings, Adverse reactions | 197698 197699 197700 197701 8VZV102JFY |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.