Ondansetron

Orange BookUNIISPLATC A04AA01

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeA04AA01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 10

ndc11
7133597260
90 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-0)
ndc11
7133597261
30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-1)
ndc11
7133597262
20 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-2)
ndc11
7133597263
10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-3)
ndc11
7133597264
6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-4)
ndc11
7133597265
60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-5)
ndc11
7133597266
9 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-6)
ndc11
7133597267
5 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-7)
ndc11
7133597268
15 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-8)
ndc11
7133597269
3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-9726-9)

Annotations

UNII (FDA Substance ID)

4AF302ESOS

ONDANSETRON

RxCUI 26225

Orange Book

A078152

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": "71335-9726_312be717-1f36-4d21-a99c-0a125764618a",
  "productndc": "71335-9726",
  "dosage_form": "TABLET, ORALLY DISINTEGRATING",
  "orange_book": {
    "appl_no": "078152",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "4MG",
        "product_no": "001",
        "approval_date": "Jun 27, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "8MG",
        "product_no": "002",
        "approval_date": "Jun 27, 2007"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ONDANSETRON",
  "proprietary_name": "Ondansetron",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA078152",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ondansetron",
  "start_marketing_date": "20070627",
  "active_numerator_strength": "4"
}

Related drugs

Other records sharing ATC code A04AA01.

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