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
7133517310
3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-0)
ndc11
7133517311
30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-1)
ndc11
7133517312
10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-2)
ndc11
7133517313
5 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-3)
ndc11
7133517314
4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-4)
ndc11
7133517315
6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-5)
ndc11
7133517316
14 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-6)
ndc11
7133517317
60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-7)
ndc11
7133517318
12 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-8)
ndc11
7133517319
90 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-9)

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": "71335-1731_bc491a5a-1f19-4c2b-85f3-459d571603a8",
  "productndc": "71335-1731",
  "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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