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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

  • ndc11
    6818087373
    3 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
}

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