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United States · US · US:65219-028_8b68715d-8b5a-473f-90fb-453ba4267b84

Ganirelix Acetate

Orange BookUNIISPLATC H01CC01

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

Identification

ManufacturerFresenius Kabi USA, LLC
CountryUS (United States)
ATC codeH01CC01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    6521902805
    1 SYRINGE, GLASS in 1 CARTON (65219-028-05) / 1 mL in 1 SYRINGE, GLASS

Annotations

UNII (FDA Substance ID)
56U7906FQW
GANIRELIX ACETATE
RxCUI 259264
Orange Book
A215658
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "56U7906FQW",
    "rxcui": "259264",
    "inchikey": "OVBICQMTCPFEBS-SATRDZAXSA-N",
    "display_name": "GANIRELIX ACETATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBCUTANEOUS",
  "spl_meta": {
    "420ce739-2756-4fb4-8a4e-5fab501ab973": {
      "match": "brand_token",
      "title": "GANIRELIX ACETATE INJECTION, SOLUTION [MULLAN PHARMACEUTICAL INC.]",
      "spl_version": "2",
      "published_date": "2026-05-13"
    }
  },
  "productid": "65219-028_8b68715d-8b5a-473f-90fb-453ba4267b84",
  "productndc": "65219-028",
  "dosage_form": "INJECTION",
  "orange_book": {
    "appl_no": "215658",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AP",
        "strength": "250MCG/0.5ML",
        "product_no": "001",
        "approval_date": "Feb 28, 2023"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "GANIRELIX ACETATE",
  "proprietary_name": "Ganirelix Acetate",
  "active_ingred_unit": "ug/.5mL",
  "application_number": "ANDA215658",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ganirelix Acetate",
  "start_marketing_date": "20230324",
  "active_numerator_strength": "250"
}

Related drugs

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