Danazol

UNIISPLATC G03XA01

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerProficient Rx LP

CountryUS (United States)

ATC codeG03XA01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 6

ndc11
7120586100
100 CAPSULE in 1 BOTTLE (71205-861-00)
ndc11
7120586130
30 CAPSULE in 1 BOTTLE (71205-861-30)
ndc11
7120586155
500 CAPSULE in 1 BOTTLE (71205-861-55)
ndc11
7120586160
60 CAPSULE in 1 BOTTLE (71205-861-60)
ndc11
7120586172
120 CAPSULE in 1 BOTTLE (71205-861-72)
ndc11
7120586190
90 CAPSULE in 1 BOTTLE (71205-861-90)

Annotations

UNII (FDA Substance ID)

N29QWW3BUO

DANAZOL

RxCUI 3102

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "N29QWW3BUO",
    "rxcui": "3102",
    "inchikey": "POZRVZJJTULAOH-LHZXLZLDSA-N",
    "display_name": "DANAZOL",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "e19acee5-ff33-45a5-bbbf-801756bc59b4": {
      "match": "brand_token",
      "title": "DANAZOL CAPSULE [TEVA PHARMACEUTICALS USA, INC.]",
      "spl_version": "15",
      "published_date": "2025-03-24"
    }
  },
  "productid": "71205-861_9e103cf9-f075-48ba-8913-2e44f9442781",
  "productndc": "71205-861",
  "dosage_form": "CAPSULE",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DANAZOL",
  "proprietary_name": "Danazol",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA078214",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Danazol",
  "start_marketing_date": "20070419",
  "active_numerator_strength": "100"
}

Related drugs

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