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United States · US · US:51672-2002_390cee55-c38f-accf-e063-6294a90ab7f7
Clotrimazole
UNIISPLATC A01AB18
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeA01AB18
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1151672200211 TUBE in 1 CARTON (51672-2002-1) / 15 g in 1 TUBE
- ndc1151672200221 TUBE in 1 CARTON (51672-2002-2) / 30 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
G07GZ97H65
CLOTRIMAZOLE
RxCUI 2623
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "G07GZ97H65",
"rxcui": "2623",
"inchikey": "VNFPBHJOKIVQEB-UHFFFAOYSA-N",
"display_name": "CLOTRIMAZOLE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"a6ac4020-2c67-426a-8289-7e54ce43d0c9": {
"match": "brand_token",
"title": "CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE CREAM [ACTAVIS PHARMA, INC.]",
"spl_version": "15",
"published_date": "2026-05-20"
}
},
"productid": "51672-2002_390cee55-c38f-accf-e063-6294a90ab7f7",
"productndc": "51672-2002",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CLOTRIMAZOLE",
"proprietary_name": "Clotrimazole",
"active_ingred_unit": "g/100g",
"application_number": "M005",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Clotrimazole",
"start_marketing_date": "19950601",
"active_numerator_strength": "1"
}Related drugs
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