NDC 70710-1140-01 - 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
- 70710-1140
- Requested NDC
- 70710-1140-01
- Package NDCs from labels
- 70710-1140-3, 70710-1140-1, 70710-1140-5, 70710-1140-4, 70710-1140-01
- Manufacturer
- Preferred Pharmaceuticals Inc.
- Effective date
- 2026-08-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Fluconazole Tablets, USP Rx only | Preferred Pharmaceuticals Inc. | 2026-08-20 | HUMAN PRESCRIPTION DRUG LABEL |
| fluconazole - A-S Medication Solutions | A-S Medication Solutions | 2026-07-30 | HUMAN PRESCRIPTION DRUG LABEL |
| fluconazole - Bryant Ranch Prepack | Bryant Ranch Prepack | 2026-06-24 | HUMAN PRESCRIPTION DRUG LABEL |
| fluconazole - Zydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Limited | Zydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Limited | 2026-04-07 | HUMAN PRESCRIPTION DRUG LABEL |
| Fluconazole Tablets, USP Rx only | REMEDYREPACK INC. | 2024-09-11 | HUMAN PRESCRIPTION DRUG LABEL |
| fluconazole - RedPharm Drug | RedPharm Drug | 2024-08-15 | HUMAN PRESCRIPTION DRUG LABEL |
| Fluconazole - Direct Rx | Direct Rx | 2024-01-09 | HUMAN PRESCRIPTION DRUG LABEL |
| Fluconazole Tablets, USP Rx only | Preferred Pharmaceuticals Inc. | 2023-06-08 | HUMAN PRESCRIPTION DRUG LABEL |
| Fluconazole Tablets, USP Rx only | NuCare Pharmaceuticals,Inc. | 2022-01-03 | HUMAN PRESCRIPTION DRUG LABEL |
| fluconazole - Proficient Rx LP | Proficient Rx LP | 2020-03-01 | HUMAN PRESCRIPTION DRUG LABEL |
| fluconazole - Bryant Ranch Prepack | Bryant Ranch Prepack | 2019-08-07 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1140-1 | fluconazole | 100 in 1 BOTTLE | TABLET | 100 | 13 | |
| 70710-1140-3 | fluconazole | 30 in 1 BOTTLE | TABLET | 30 | 13 | |
| 70710-1140-4 | fluconazole | 10 in 1 BLISTER PACK | TABLET | 10 | 13 | |
| 70710-1140-4 | fluconazole | 10 in 1 CARTON | TABLET | 10 | 13 | |
| 70710-1140-5 | fluconazole | 500 in 1 BOTTLE | TABLET | 500 | 13 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1140 | FLUCONAZOLE TABLET [ZYDUS PHARMACEUTICALS (USA) INC.] | 12 | Current NDC, Legacy NDC, 5 package rows | 20240306_d1364455-1537-46d4-b093-38cca3be778f.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70710-1140-1 | EA - Each | 70710-1140 | 661b5f73-5fe3-425b-8a7f-c5c384fc2104 | 1 | 2018-02-20 |
| 70710-1140-3 | EA - Each | 70710-1140 | f43ad117-c887-4f28-851a-6e9aea4c970f | 1 | 2018-02-20 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| FLUCONAZOLE | ACTIVE INGREDIENT | 8VZV102JFY | DIRECT RX (FLUCONAZOLE) TABLET [DIRECT RX] | 1 | |
| FLUCONAZOLE | ACTIVE MOIETY | 8VZV102JFY | DIRECT RX (FLUCONAZOLE) TABLET [DIRECT RX] | 1 | |
| ANHYDROUS DIBASIC CALCIUM PHOSPHATE | INACTIVE INGREDIENT | L11K75P92J | DIRECT RX (FLUCONAZOLE) TABLET [DIRECT RX] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | DIRECT RX (FLUCONAZOLE) TABLET [DIRECT RX] | 1 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | DIRECT RX (FLUCONAZOLE) TABLET [DIRECT RX] | 1 | |
| magnesium stearate | INACTIVE INGREDIENT | 70097M6I30 | DIRECT RX (FLUCONAZOLE) TABLET [DIRECT RX] | 1 | |
| povidone | INACTIVE INGREDIENT | FZ989GH94E | DIRECT RX (FLUCONAZOLE) TABLET [DIRECT RX] | 1 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | DIRECT RX (FLUCONAZOLE) TABLET [DIRECT RX] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | DIRECT RX (FLUCONAZOLE) TABLET [DIRECT RX] | 1 |
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 |
|---|---|---|---|---|---|---|
| Calamine Plus Pramoxine HCl | CALAMINE PLUS SPRAY | HY-VEE, INC | 415ecfe9-3145-f23e-e063-6394a90adfd8 | 2025-11-17 | Warnings | 1K09F3G675 |
| Au Kah Chuen Fugical | CALAMINE AND DIPHENHYDRAMINE HYDROCHLORID | Zhejiang Dingtai Pharmaceutical Co., Ltd | 5b4add17-6c3d-4093-826a-2edb41c1d1db | 2025-11-10 | Warnings | 1K09F3G675 |
| FARGELIN HEMORRHOIDAL | CALAMINE, PETROLATUM AND PHENYLEPHRINE HYDROCHLORIDE | MADISON ONE ACME INC | 6844ad63-512d-496a-9458-011894185b0d | 2025-11-10 | Warnings | 1K09F3G675 |
| Calamine Plus | CALAMINE PLUS PRAMOXINE HCL | Chain Drug Marketing Association Inc | 1a3f8819-58cf-8923-e063-6394a90a37af | 2025-11-06 | Warnings | 1K09F3G675 |
| Calamine Plus Pramoxine HCl | CALAMINE PLUS NO TOUCH SPRAY | Premier Brands of America Inc. | 36481d67-2346-470b-e063-6294a90aae99 | 2025-11-03 | Warnings | 1K09F3G675 |
| Calamine Plus | CALAMINE PLUS PRAMOXINE HCL | AmerisourceBergen Drug Corporation | f161e151-4fab-2fbc-e053-2a95a90a5437 | 2025-10-30 | Warnings | 1K09F3G675 |
| REMEDY Calazime Skin Protectant | CALAMINE, MENTHOL, WHITE PETROLATUM, ZINC OXIDE | Medline Industries, LP | 1295cfcc-5b61-481b-964b-f53ffd0cb58e | 2025-10-30 | Warnings | 1K09F3G675 |
| Calamine Plus | CALAMINE PLUS PRAMOXINE HCL | Meijer Distribution Inc. | 03c46823-0b1f-4101-e063-6294a90aaf94 | 2025-10-30 | Warnings | 1K09F3G675 |
| Aveeno Anti-Itch Concentrated | ZINC OXIDE, FERRIC OXIDE RED, AND PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | 07f4d4d0-9cee-46c3-bc71-2024abd31c9e | 2025-10-29 | Warnings | 1K09F3G675 |
| LACRIFRESH HYDRAPF | GLYCERIN, POVIDONE | AVIZOR, S.A. | 41bbd23e-0ec8-eb18-e063-6294a90a46d1 | 2025-10-27 | Warnings | FZ989GH94E |
| LACRIFRESH HYDRAMAXPF | GLYCERIN, POVIDONE | AVIZOR, S.A. | 41be1604-89b4-7ec3-e063-6294a90a3331 | 2025-10-27 | Warnings | FZ989GH94E |
| Calamine Plus Pramoxine HCl | CALAMINE PLUS SPRAY | Premier Brands of America, Inc. | d3452573-f91f-f157-e053-2a95a90a1ad8 | 2025-10-27 | Warnings | 1K09F3G675 |
| Stye | POLYVINYL ALCOHOL AND POVIDONE | Medtech Products Inc. | 60c11d3d-df20-4d1c-b425-49a84fecea30 | 2025-10-23 | Warnings | FZ989GH94E |
| iVIZIA Dry Eye | POVIDONE | Thea Pharma Inc. | 1ef73cb1-da48-a713-e063-6294a90afa9d | 2025-10-20 | Warnings | FZ989GH94E |
| Fluconazole | FLUCONAZOLE | PD-Rx Pharmaceuticals, Inc. | 28d53f27-a0cd-4d8d-e054-00144ff8d46c | 2025-10-15 | Warnings, Adverse reactions | 197698 8VZV102JFY |
| Fluconazole | FLUCONAZOLE | Bryant Ranch Prepack | 701cd91f-4f79-48a7-8fe5-a9678d7a4ac8 | 2025-10-06 | Warnings, Adverse reactions | 197698 8VZV102JFY |
| Fluconazole | FLUCONAZOLE | Dr. Reddy's Laboratories Limited | d7fa1d79-4cd3-4a55-b74b-b31e82e616a3 | 2025-09-23 | Warnings, Adverse reactions | ANDA076658 197698 197699 197700 197701 8VZV102JFY |
| Eyes Irritation Relief | POLYVINYL ALCOHOL AND POVIDONE AND TETRAHYDROZOLINE HYDROCHLORIDE | CARDINAL HEALTH 110, LLC. DBA LEADER | bd2608c6-ffdf-352a-e053-2995a90a26a8 | 2025-09-12 | Warnings | FZ989GH94E |
| Powder | TITANIUM DIOXIDE | Oxygen Development LLC | 08b52f29-c1a0-c673-e063-6294a90a9a7a | 2025-09-05 | Warnings | 1K09F3G675 |
| Powder | TITANIUM DIOXIDE | Oxygen Development LLC | 08b8003f-40be-3380-e063-6294a90a4f6b | 2025-09-05 | Warnings | 1K09F3G675 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.