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United States · US · US:68180-873_a3be3d49-c5f9-4700-b928-317b0289391f
WYMZYA Fe
Orange BookSPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLupin Pharmaceuticals, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1168180873733 POUCH in 1 CARTON (68180-873-73) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACK * 21 TABLET, CHEWABLE in 1 BLISTER PACK (68180-832-74) * 7 TABLET in 1 BLISTER PACK (68180-856-74)
Annotations
Orange Book
A091332
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"4f824b11-14f3-4a92-a516-562b3a434df0": {
"match": "brand_token",
"title": "WYMZYA FE (NORETHINDRONE AND ETHINYL ESTRADIOL) KIT [LUPIN PHARMACEUTICALS, INC.]",
"spl_version": "15",
"published_date": "2025-11-20"
}
},
"productid": "68180-873_a3be3d49-c5f9-4700-b928-317b0289391f",
"productndc": "68180-873",
"dosage_form": "KIT",
"orange_book": {
"appl_no": "091332",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.035MG;0.4MG",
"product_no": "001",
"approval_date": "Mar 23, 2016"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": null,
"proprietary_name": "WYMZYA Fe",
"active_ingred_unit": null,
"application_number": "ANDA091332",
"marketing_category": "ANDA",
"nonproprietary_name": "NORETHINDRONE AND ETHINYL ESTRADIOL",
"start_marketing_date": "20201130",
"active_numerator_strength": null
}Access this data programmatically
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