🇺🇸
United States · US · US:71205-757_637718aa-a453-4acd-a992-590d637b63a3
Minoxidil
Orange BookUNIISPLATC C02DC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeC02DC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11712057573030 TABLET in 1 BOTTLE, PLASTIC (71205-757-30)
- ndc11712057576060 TABLET in 1 BOTTLE, PLASTIC (71205-757-60)
- ndc11712057579090 TABLET in 1 BOTTLE, PLASTIC (71205-757-90)
Annotations
UNII (FDA Substance ID)
5965120SH1
MINOXIDIL
RxCUI 6984
Orange Book
A071344
AB
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": "ORAL",
"spl_meta": {
"1b54eca8-4a96-1b5e-e063-6394a90a7b94": {
"match": "brand_token",
"title": "MINOXIDIL (MINOXIDIL FOAM 5% (WOMENS)) AEROSOL, FOAM [CLARITY COSMETICS INC.]",
"spl_version": "2",
"published_date": "2026-06-02"
}
},
"productid": "71205-757_637718aa-a453-4acd-a992-590d637b63a3",
"productndc": "71205-757",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "071344",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "2.5MG",
"product_no": "001",
"approval_date": "Mar 3, 1987"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "MINOXIDIL",
"proprietary_name": "Minoxidil",
"active_ingred_unit": "mg/1",
"application_number": "ANDA071344",
"marketing_category": "ANDA",
"nonproprietary_name": "Minoxidil",
"start_marketing_date": "20091026",
"active_numerator_strength": "2.5"
}Related drugs
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