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United States · US · US:51672-1359_38efa4f4-a3f2-fd03-e063-6394a90aac00
Oxiconazole Nitrate
Orange BookUNIISPLATC G01AF17
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeG01AF17
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1151672135911 TUBE in 1 CARTON (51672-1359-1) / 15 g in 1 TUBE
- ndc1151672135921 TUBE in 1 CARTON (51672-1359-2) / 30 g in 1 TUBE
- ndc1151672135931 TUBE in 1 CARTON (51672-1359-3) / 60 g in 1 TUBE
- ndc1151672135981 TUBE in 1 CARTON (51672-1359-8) / 90 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
RQ8UL4C17S
OXICONAZOLE NITRATE
RxCUI 56226
Orange Book
A205076
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "RQ8UL4C17S",
"rxcui": "56226",
"inchikey": "WVNOAGNOIPTWPT-NDUABGMUSA-N",
"display_name": "OXICONAZOLE NITRATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"aa368d2b-a5d2-49dd-86e1-5693b68b46f4": {
"match": "brand_token",
"title": "OXICONAZOLE NITRATE CREAM [E. FOUGERA & CO. A DIVISION OF FOUGERA PHARMACEUTICALS, LLC]",
"spl_version": "5",
"published_date": "2026-04-02"
}
},
"productid": "51672-1359_38efa4f4-a3f2-fd03-e063-6394a90aac00",
"productndc": "51672-1359",
"dosage_form": "CREAM",
"orange_book": {
"appl_no": "205076",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 1% BASE",
"product_no": "001",
"approval_date": "Mar 7, 2016"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "OXICONAZOLE NITRATE",
"proprietary_name": "Oxiconazole Nitrate",
"active_ingred_unit": "mg/g",
"application_number": "ANDA205076",
"marketing_category": "ANDA",
"nonproprietary_name": "Oxiconazole Nitrate",
"start_marketing_date": "20160307",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code G01AF17.
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