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United States · US · US:56104-253_3bba5b9f-d184-6f93-e063-6394a90ae951
Anti- Fungal Miconazole Nitrate
UNIISPLATC G01AF04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPremier Brands of America Inc.
CountryUS (United States)
ATC codeG01AF04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11561042530171 g in 1 BOTTLE, PLASTIC (56104-253-01)
Annotations
UNII (FDA Substance ID)
VW4H1CYW1K
MICONAZOLE NITRATE
RxCUI 42790
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "VW4H1CYW1K",
"rxcui": "42790",
"inchikey": "MCCACAIVAXEFAL-UHFFFAOYSA-N",
"display_name": "MICONAZOLE NITRATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"f186bdc1-db6c-0fab-e053-2995a90a7c58": {
"match": "brand_token",
"title": "ANTI- FUNGAL MICONAZOLE NITRATE (MICONAZOLE NITRATE) POWDER [PREMIER BRANDS OF AMERICA INC.]",
"spl_version": "7",
"published_date": "2025-08-08"
}
},
"productid": "56104-253_3bba5b9f-d184-6f93-e063-6394a90ae951",
"productndc": "56104-253",
"dosage_form": "POWDER",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MICONAZOLE NITRATE",
"proprietary_name": "Anti- Fungal Miconazole Nitrate",
"active_ingred_unit": "g/71g",
"application_number": "M005",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Miconazole Nitrate",
"start_marketing_date": "20220411",
"active_numerator_strength": "1.42"
}Related drugs
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