Cytarabine

Orange BookUNIISPLATC L01BC01

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerMeitheal Pharmaceuticals Inc.

CountryUS (United States)

ATC codeL01BC01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7128810806
5 VIAL, SINGLE-DOSE in 1 CARTON (71288-108-06) / 5 mL in 1 VIAL, SINGLE-DOSE (71288-108-05)

Annotations

UNII (FDA Substance ID)

04079A1RDZ

CYTARABINE

RxCUI 3041

Orange Book

A206189

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "04079A1RDZ",
    "rxcui": "3041",
    "inchikey": "UHDGCWIWMRVCDJ-CCXZUQQUSA-N",
    "display_name": "CYTARABINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRATHECAL; INTRAVENOUS; SUBCUTANEOUS",
  "spl_meta": {
    "277597b0-7d85-40a3-a34a-70c6a883fc6d": {
      "match": "brand_token",
      "title": "CYTARABINE INJECTION, SOLUTION [HOSPIRA, INC.]",
      "spl_version": "13",
      "published_date": "2025-09-01"
    }
  },
  "productid": "71288-108_ba035466-3b01-4e2b-abf5-d876619a2674",
  "productndc": "71288-108",
  "dosage_form": "INJECTION, SOLUTION",
  "orange_book": {
    "appl_no": "206189",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "20MG/ML",
        "product_no": "001",
        "approval_date": "Jun 26, 2020"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CYTARABINE",
  "proprietary_name": "Cytarabine",
  "active_ingred_unit": "mg/mL",
  "application_number": "ANDA206189",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Cytarabine",
  "start_marketing_date": "20200626",
  "active_numerator_strength": "20"
}

Related drugs

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