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United States · US · US:71205-713_35203011-d93c-4169-a9cb-90b6d20b146b

Ondansetron

Orange BookUNIISPLATC A04AA01

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

Identification

ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeA04AA01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 5

  • ndc11
    7120571310
    1 BLISTER PACK in 1 BAG (71205-713-10) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
  • ndc11
    7120571320
    2 BLISTER PACK in 1 BAG (71205-713-20) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
  • ndc11
    7120571330
    30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71205-713-30)
  • ndc11
    7120571360
    60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71205-713-60)
  • ndc11
    7120571390
    90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71205-713-90)

Annotations

UNII (FDA Substance ID)
4AF302ESOS
ONDANSETRON
RxCUI 26225
Orange Book
A090469
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "4AF302ESOS",
    "rxcui": "26225",
    "inchikey": "FELGMEQIXOGIFQ-UHFFFAOYSA-N",
    "display_name": "ONDANSETRON",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "d62cd60b-f87e-4825-bead-1d18bbc4e480": {
      "match": "brand_token",
      "title": "ONDANSETRON INJECTION, SOLUTION [HOSPIRA, INC.]",
      "spl_version": "4",
      "published_date": "2026-05-25"
    }
  },
  "productid": "71205-713_35203011-d93c-4169-a9cb-90b6d20b146b",
  "productndc": "71205-713",
  "dosage_form": "TABLET, ORALLY DISINTEGRATING",
  "orange_book": {
    "appl_no": "090469",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "4MG",
        "product_no": "001",
        "approval_date": "Apr 12, 2010"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "8MG",
        "product_no": "002",
        "approval_date": "Apr 12, 2010"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ONDANSETRON",
  "proprietary_name": "Ondansetron",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA090469",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ondansetron",
  "start_marketing_date": "20100412",
  "active_numerator_strength": "8"
}

Related drugs

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