NDC 51672-2001-01 - Miconazole Nitrate
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
- 51672-2001
- Requested NDC
- 51672-2001-01
- Package NDCs from labels
- 51672-2001-1, 51672-2001-2, 51672-2001-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.
- Effective date
- 2026-08-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Miconazole Nitrate | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | 2026-08-25 | HUMAN OTC DRUG LABEL |
| Miconazole Nitrate - A-S Medication Solutions | A-S Medication Solutions | 2025-12-03 | HUMAN OTC DRUG LABEL |
| Miconazole Nitrate - A-S Medication Solutions | A-S Medication Solutions | 2025-02-24 | HUMAN OTC DRUG LABEL |
| Miconazole Nitrate | NuCare Pharmaceuticals,Inc. | 2022-03-15 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-2001-1 | Miconazole Nitrate | 1 in 1 CARTON | CREAM | 1 | 5 | |
| 51672-2001-1 | Miconazole Nitrate | 15 g in 1 TUBE | CREAM | 15 | 5 | |
| 51672-2001-2 | Miconazole Nitrate | 1 in 1 CARTON | CREAM | 1 | 5 | |
| 51672-2001-2 | Miconazole Nitrate | 30 g in 1 TUBE | CREAM | 30 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-2001 | MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] | 4 | Current NDC, Legacy NDC, 4 package rows | 20241222_7fd4037e-d350-47b7-a7d9-a43b8e366fa0.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-2001-1 | GM - Gram | 51672-2001 | 9dbd7e37-8219-4939-b49c-0359e914af97 | 1 | 2012-07-24 |
| 51672-2001-2 | GM - Gram | 51672-2001 | 9cf50338-1157-450f-91bd-7c055b0d4948 | 1 | 2013-02-13 |
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 |
|---|---|---|---|---|---|---|
| Anti-Fungal Powder | MICONAZOLE NITRATE | TopCo Associates | 19c3fbc5-abde-57df-e063-6394a90a125c | 2025-11-06 | Warnings | M005 VW4H1CYW1K |
| Tolnaftate | FOOT ODOR CONTROL SPRAY | Topco Associates LLC | 17993a9f-0d44-43a1-8608-94ee8a08b539 | 2025-11-06 | Warnings | M005 |
| DVO Estriol cream | ESTRIOL0.2% | Guangzhou Huixue Biotechnology Co., Ltd. | 42e4cc84-7c00-6937-e063-6294a90a0c09 | 2025-11-05 | Warnings | M005 |
| Bacteriostatic Water | BACTERIOSTATIC WATER | ProPharma Distribution | 42c6938e-f747-ae13-e063-6294a90a59a3 | 2025-11-04 | Warnings, Adverse reactions | 059QF0KO0R |
| Medline | MICONAZOL NITRATE | Medline Industries, LP | dad58efb-cc20-577a-e053-2a95a90abd9d | 2025-11-03 | Warnings | M005 VW4H1CYW1K |
| Tolnafate | TOLNAFTATE POWDER SPRAY | HEB | c6af941a-0b85-4611-a6f3-b13fcf3c4a87 | 2025-11-03 | Warnings | M005 |
| Tolnaftate | FOOT ODOR CONTROL SPRAY | HEB | c585605b-ecb8-4dd8-9205-a9be02d751fa | 2025-11-03 | Warnings | M005 |
| Premier Solutions Antifungal Tolnaftate Liquid | TOLNAFTATE | Premier Brands of America, Inc. | e1971c1c-5687-577b-e053-2a95a90ad95f | 2025-11-03 | Warnings | M005 |
| Miconazole nitrate | ANTIFUNGAL MICONAZOLE LIQUID CONTINUOUS SPRAY | Premier Brands of America Inc. | 3803c643-35d1-06d4-e063-6294a90ac6f6 | 2025-11-03 | Warnings | M005 VW4H1CYW1K |
| Sterile Water | WATER | ICU Medical Inc. | aab10f03-26ae-4dbc-a481-ef025e48b405 | 2025-11-02 | Warnings, Adverse reactions | 059QF0KO0R |
| Sterile Water | WATER | ICU Medical Inc. | e3484bc6-ed7f-43ef-9d49-c131a8dff2dd | 2025-11-02 | Warnings, Adverse reactions | 059QF0KO0R |
| dg health miconazole 3 | MICONAZOLE NITRATE | Dolgencorp Inc | d84aa78d-b408-4d51-a54c-c66f6cef33f1 | 2025-11-01 | Warnings | 998483 |
| Anti-fungal Powder Miconazole Nitrate | MICONAZOLE NITRATE | Meijer Distribution Inc | 03fd069d-685d-b8ac-e063-6394a90a31f8 | 2025-10-31 | Warnings | M005 VW4H1CYW1K |
| Tolnaftate | ANTIFUNGAL LIQUID SPRAY | Premier Brands of America Inc. | 7a6a63cd-e87d-4229-8acf-b65d63909eb6 | 2025-10-31 | Warnings | M005 |
| miconazole 3 | MICONAZOLE NITRATE | H E B | f24ec8b6-0d2a-4bf0-9f2b-cad5bee9aaa6 | 2025-10-31 | Warnings | 998483 |
| Azolen | MICONAZOLE NITRATE | Stratus Pharmaceuticals, Inc. | 9c2574f3-3be4-405a-9c87-943dc6ef8777 | 2025-10-30 | Warnings | M005 VW4H1CYW1K |
| Family Care Antifungal | CLOTRIMAZOLE | United Exchange Corp. | 63255079-ecf1-1e77-e053-2a91aa0a7b6c | 2025-10-30 | Warnings | M005 |
| GNP Hemorrhoidal | MINERAL OIL, PETROLATUM, PHENYLEPHRINE, HCL | Amerisource Bergen | b0f0ef97-9add-717f-e053-2a95a90a0eb0 | 2025-10-30 | Warnings | T5L8T28FGP |
| Miconazorb AF | MICONAZOLE NITRATE | AmerisourceBergen Drug Corporation | 13a20d21-42d5-fe56-e063-6394a90aaf57 | 2025-10-30 | Warnings | M005 VW4H1CYW1K |
| Antifungal Liquid Continuous | MICONAZOLE NITRATE | Family Dollar Services, Inc | 17cc4601-f946-df8b-e063-6394a90a3897 | 2025-10-30 | Warnings | M005 VW4H1CYW1K |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.