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
7133501320
60 TABLET, FILM COATED in 1 BOTTLE (71335-0132-0)
ndc11
7133501321
10 TABLET, FILM COATED in 1 BOTTLE (71335-0132-1)
ndc11
7133501322
3 TABLET, FILM COATED in 1 BOTTLE (71335-0132-2)
ndc11
7133501323
30 TABLET, FILM COATED in 1 BOTTLE (71335-0132-3)
ndc11
7133501324
15 TABLET, FILM COATED in 1 BOTTLE (71335-0132-4)
ndc11
7133501325
6 TABLET, FILM COATED in 1 BOTTLE (71335-0132-5)
ndc11
7133501326
4 TABLET, FILM COATED in 1 BOTTLE (71335-0132-6)
ndc11
7133501327
90 TABLET, FILM COATED in 1 BOTTLE (71335-0132-7)
ndc11
7133501328
12 TABLET, FILM COATED in 1 BOTTLE (71335-0132-8)
ndc11
7133501329
20 TABLET, FILM COATED in 1 BOTTLE (71335-0132-9)

Annotations

UNII (FDA Substance ID)

NMH84OZK2B

ONDANSETRON HYDROCHLORIDE

RxCUI 203148

Orange Book

A077851

ABAB

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": "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": "71335-0132_aba5e1a7-a00a-4e76-b0e3-dfbe4179eec0",
  "productndc": "71335-0132",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "077851",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 4MG BASE",
        "product_no": "001",
        "approval_date": "Jun 25, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 8MG BASE",
        "product_no": "002",
        "approval_date": "Jun 25, 2007"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ONDANSETRON HYDROCHLORIDE",
  "proprietary_name": "Ondansetron",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA077851",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ondansetron",
  "start_marketing_date": "20070727",
  "active_numerator_strength": "4"
}

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