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
7133513140
90 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1314-0)
ndc11
7133513141
30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1314-1)
ndc11
7133513142
20 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1314-2)
ndc11
7133513143
10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1314-3)
ndc11
7133513144
6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1314-4)
ndc11
7133513145
60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1314-5)
ndc11
7133513146
9 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1314-6)
ndc11
7133513147
5 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1314-7)
ndc11
7133513148
15 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1314-8)
ndc11
7133513149
3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1314-9)

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": "71335-1314_b16468ac-e482-41d2-ac22-966ad7807bcf",
  "productndc": "71335-1314",
  "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": "4"
}

Related drugs

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