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United States · US · US:0430-0420_4b7cbcd3-7192-43cf-bd16-98bc8ed95645
Lo Loestrin Fe
Orange BookSPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllergan, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1104300420145 BLISTER PACK in 1 CARTON (0430-0420-14) / 1 KIT in 1 BLISTER PACK
- ndc1104300420608 CARTON in 1 TRAY (0430-0420-60) / 30 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK
- ndc1104300420956 CARTON in 1 TRAY (0430-0420-95) / 1 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK
Annotations
Orange Book
N022501
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"c33072cf-625d-4b4a-981e-ec049c5d78aa": {
"match": "brand_token",
"title": "LO LOESTRIN FE (NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL, ETHINYL ESTRADIOL AND FERROUS FUMARATE) KIT [ALLERGAN, INC.]",
"spl_version": "24",
"published_date": "2025-03-12"
}
},
"productid": "0430-0420_4b7cbcd3-7192-43cf-bd16-98bc8ed95645",
"productndc": "0430-0420",
"dosage_form": "KIT",
"orange_book": {
"appl_no": "022501",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "0.01MG,0.01MG;1MG,N/A",
"product_no": "001",
"approval_date": "Oct 21, 2010"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": null,
"proprietary_name": "Lo Loestrin Fe",
"active_ingred_unit": null,
"application_number": "NDA022501",
"marketing_category": "NDA",
"nonproprietary_name": "norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate",
"start_marketing_date": "20101201",
"active_numerator_strength": null
}Access this data programmatically
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