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
7133506500
90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0650-0)
ndc11
7133506501
30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0650-1)
ndc11
7133506502
20 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0650-2)
ndc11
7133506503
10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0650-3)
ndc11
7133506504
6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0650-4)
ndc11
7133506505
60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0650-5)
ndc11
7133506506
9 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0650-6)
ndc11
7133506507
5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0650-7)
ndc11
7133506508
15 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0650-8)
ndc11
7133506509
3 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0650-9)

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": "71335-0650_e5cd8042-5934-4ebf-98f2-90e3d5b48beb",
  "productndc": "71335-0650",
  "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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