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United States · US · US:11673-426_a7cd1ad8-786a-460d-83d7-57d2e0dee5fb

Up and up tioconazole 1

Orange BookUNIISPLATC G01AF08

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerTarget Corporation
CountryUS (United States)
ATC codeG01AF08
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    1167342654
    1 POUCH in 1 CARTON (11673-426-54) / 1 APPLICATOR in 1 POUCH / 4.6 g in 1 APPLICATOR

Annotations

UNII (FDA Substance ID)
S57Y5X1117
TIOCONAZOLE
RxCUI 38298
Orange Book
A075915
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "S57Y5X1117",
    "rxcui": "38298",
    "inchikey": "QXHHHPZILQDDPS-UHFFFAOYSA-N",
    "display_name": "TIOCONAZOLE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "VAGINAL",
  "spl_meta": {
    "51c0a953-93cb-4d0a-b51c-02d9482d1746": {
      "match": "brand_token",
      "title": "UP AND UP ALLERGY RELIEF NASAL (FLUTICASONE PROPIONATE) SPRAY, METERED [TARGET CORPORATION]",
      "spl_version": "12",
      "published_date": "2026-05-13"
    }
  },
  "productid": "11673-426_a7cd1ad8-786a-460d-83d7-57d2e0dee5fb",
  "productndc": "11673-426",
  "dosage_form": "OINTMENT",
  "orange_book": {
    "appl_no": "075915",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "6.5%",
        "product_no": "001",
        "approval_date": "Nov 21, 2001"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TIOCONAZOLE",
  "proprietary_name": "Up and up tioconazole 1",
  "active_ingred_unit": "g/100g",
  "application_number": "ANDA075915",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Tioconazole",
  "start_marketing_date": "20090708",
  "active_numerator_strength": "6.5"
}

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