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United States · US · US:72572-520_0c34b5a6-e21b-41e7-8e7b-61a9706b67e0

Ondansetron

Orange BookUNIISPLATC A04AA01

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerCivica, Inc.
CountryUS (United States)
ATC codeA04AA01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7257252025
    25 VIAL in 1 CARTON (72572-520-25) / 2 mL in 1 VIAL (72572-520-01)

Annotations

UNII (FDA Substance ID)
NMH84OZK2B
ONDANSETRON HYDROCHLORIDE
RxCUI 203148
Orange Book
A077541
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "NMH84OZK2B",
    "rxcui": "203148",
    "inchikey": "VRSLTNZJOUZKLX-UHFFFAOYSA-N",
    "display_name": "ONDANSETRON HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAMUSCULAR; INTRAVENOUS",
  "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": "72572-520_0c34b5a6-e21b-41e7-8e7b-61a9706b67e0",
  "productndc": "72572-520",
  "dosage_form": "INJECTION",
  "orange_book": {
    "appl_no": "077541",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AP",
        "strength": "EQ 2MG BASE/ML",
        "product_no": "001",
        "approval_date": "Dec 26, 2006"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ONDANSETRON HYDROCHLORIDE",
  "proprietary_name": "Ondansetron",
  "active_ingred_unit": "mg/mL",
  "application_number": "ANDA077541",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ondansetron",
  "start_marketing_date": "20191118",
  "active_numerator_strength": "2"
}

Related drugs

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