🇺🇸
United States · US · US:70000-0653_cf5fb0e6-c973-4bd4-a03e-96822c7585a7
Leader Minoxidil
Orange BookUNIISPLATC C02DC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCardinal Health 110, LLC. dba Leader
CountryUS (United States)
ATC codeC02DC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1170000065313 BOTTLE, DROPPER in 1 CARTON (70000-0653-1) / 60 mL in 1 BOTTLE, DROPPER
- ndc11700000653260 mL in 1 BOTTLE, DROPPER (70000-0653-2)
Annotations
UNII (FDA Substance ID)
5965120SH1
MINOXIDIL
RxCUI 6984
Orange Book
A075598
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": {
"12971fb2-2314-4443-bf70-b7eb5859b148": {
"match": "brand_token",
"title": "LEADER MUCUS RELIEF D (GUAIFENESIN, PSEUDOEPHEDRINE HYDROCHLORIDE) TABLET, MULTILAYER, EXTENDED RELEASE [CARDINAL HEALTH 110, LLC. DBA LEADER]",
"spl_version": "3",
"published_date": "2026-06-01"
}
},
"productid": "70000-0653_cf5fb0e6-c973-4bd4-a03e-96822c7585a7",
"productndc": "70000-0653",
"dosage_form": "SOLUTION",
"orange_book": {
"appl_no": "075598",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "5%",
"product_no": "001",
"approval_date": "Jun 13, 2001"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MINOXIDIL",
"proprietary_name": "Leader Minoxidil",
"active_ingred_unit": "g/100mL",
"application_number": "ANDA075598",
"marketing_category": "ANDA",
"nonproprietary_name": "minoxidil",
"start_marketing_date": "20240304",
"active_numerator_strength": "5"
}Related drugs
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