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
7133526350
3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-2635-0)
ndc11
7133526351
30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-2635-1)
ndc11
7133526352
10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-2635-2)
ndc11
7133526353
5 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-2635-3)
ndc11
7133526354
4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-2635-4)
ndc11
7133526355
6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-2635-5)
ndc11
7133526356
14 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-2635-6)
ndc11
7133526357
60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-2635-7)
ndc11
7133526358
12 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-2635-8)
ndc11
7133526359
90 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-2635-9)

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": "71335-2635_b267b802-ee97-4554-bd6a-8b8ae3c49aba",
  "productndc": "71335-2635",
  "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": "8"
}

Related drugs

Other records sharing ATC code A04AA01.

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