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 |
|---|---|---|---|---|---|---|
| Fluconazole | FLUCONAZOLE | Proficient Rx LP | fbb1bda3-f733-4404-9c9d-46c418700c03 | 2022-08-01 | Warnings, Adverse reactions | ANDA077253 197700 8VZV102JFY |
| Fluconazole | FLUCONAZOLE | Asclemed USA, Inc. | 56a9de97-bbb9-4210-9ace-f77317d5f33b | 2022-03-04 | Warnings, Adverse reactions | ANDA077253 197699 8VZV102JFY |
| d4b2e102-9b2d-17c9-e053-2995a90a06d1 | d4b2e102-9b2c-17c9-e053-2995a90a06d1 | 2022-01-03 | Warnings, Adverse reactions | d4b2e102-9b2d-17c9-e053-2995a90a06d1 d4b2e102-9b2c-17c9-e053-2995a90a06d1 | ||
| Melange combination | CALCAREA SULPHURICA, CALCIUM PHOSPHORICUM, KALI MURIATICUM, KALIUM PHOSPHORICUM, KALI SULPHURICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRIUM SULFURICUM, CALCAREA FLUORICA, FERRUM PHOSPHORICUM, SILICEA | Seroyal USA | 0a071fbf-0075-4479-e054-00144ff8d46c | 2021-07-14 | Warnings | L11K75P92J |
| fdc2b846-5ed8-4884-aad4-6b55f374909d | 01753816-b263-4881-92a3-09b5b949781e | 2021-04-16 | Warnings, Adverse reactions | 01753816-b263-4881-92a3-09b5b949781e | ||
| MEDULLOSSEINUM PLEX | ARNICA MONTANA, CALCAREA PHOSPHORICA, CALENDULA OFFICINALIS, HYPERICUM PERFORATUM, MEDULLOSSEINUM, PULSATILLA, RUTA GRAVEOLENS, SYMPHYTUM OFFICINALE | Seroyal USA | 22b7eafe-ef76-0677-e054-00144ff88e88 | 2020-10-09 | Warnings | L11K75P92J |
| fluconazole | FLUCONAZOLE | Proficient Rx LP | f232600e-70ce-4001-b9da-31442f0920b9 | 2020-03-01 | Warnings, Adverse reactions | ANDA208963 71205-283-90 71205-283-60 71205-283-30 71205-283 197700 1410a251-cc08-49a0-b4aa-dfd217bca85b f232600e-70ce-4001-b9da-31442f0920b9 8VZV102JFY |
| fluconazole | FLUCONAZOLE | Proficient Rx LP | 7c8bb5ff-37e7-4f5e-8ea7-12269b2c7fd3 | 2019-10-01 | Warnings, Adverse reactions | ANDA208963 197699 8VZV102JFY |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.