🇺🇸
United States · US · US:70000-0600_51245457-71af-6325-e063-6394a90ade8b
LEADER Emergency Contraceptive Levonorgestrel
Orange BookUNIISPLATC G03AD01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCardinal Health 110, LLC. DBA Leader
CountryUS (United States)
ATC codeG03AD01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1170000060011 BLISTER PACK in 1 CARTON (70000-0600-1) / 1 TABLET in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
5W7SIA7YZW
LEVONORGESTREL
RxCUI 6373
Orange Book
A202635
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "5W7SIA7YZW",
"rxcui": "6373",
"inchikey": "WWYNJERNGUHSAO-XUDSTZEESA-N",
"display_name": "LEVONORGESTREL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"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": "70000-0600_51245457-71af-6325-e063-6394a90ade8b",
"productndc": "70000-0600",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "202635",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "1.5MG",
"product_no": "001",
"approval_date": "Sep 11, 2014"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LEVONORGESTREL",
"proprietary_name": "LEADER Emergency Contraceptive Levonorgestrel",
"active_ingred_unit": "mg/1",
"application_number": "ANDA202635",
"marketing_category": "ANDA",
"nonproprietary_name": "levonorgestrel",
"start_marketing_date": "20220322",
"active_numerator_strength": "1.5"
}Related drugs
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