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United States · US · US:51326-161_b2a7381d-b3ed-4db7-b7eb-06a3894ae34b
Womens Minoxidil
Orange BookUNIISPLATC C02DC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTopiderm, Inc.
CountryUS (United States)
ATC codeC02DC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11513261610160 mL in 1 BOTTLE (51326-161-01)
Annotations
UNII (FDA Substance ID)
5965120SH1
MINOXIDIL
RxCUI 6984
Orange Book
A078176
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "5965120SH1",
"rxcui": "6984",
"inchikey": "ZFMITUMMTDLWHR-UHFFFAOYSA-N",
"display_name": "MINOXIDIL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"5a6aa2df-bf69-465d-ba62-e660b13f16cd": {
"match": "brand_token",
"title": "WOMENS GENTLE LAXATIVE (BISACODYL) TABLET, DELAYED RELEASE [CHAIN DRUG MARKETING ASSOCIATION INC]",
"spl_version": "8",
"published_date": "2026-03-02"
}
},
"productid": "51326-161_b2a7381d-b3ed-4db7-b7eb-06a3894ae34b",
"productndc": "51326-161",
"dosage_form": "LIQUID",
"orange_book": {
"appl_no": "078176",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "2%",
"product_no": "001",
"approval_date": "Nov 9, 2007"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MINOXIDIL",
"proprietary_name": "Womens Minoxidil",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA078176",
"marketing_category": "ANDA",
"nonproprietary_name": "Minoxidil",
"start_marketing_date": "20210326",
"active_numerator_strength": "20"
}Related drugs
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