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United States · US · US:72603-198_5499e3f9-5d5d-4eeb-a859-62cc967d468f

Zoledronic acid

Orange BookUNIISPLATC M05BA08

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

Identification

ManufacturerNORTHSTAR RX LLC
CountryUS (United States)
ATC codeM05BA08
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7260319801
    1 VIAL, GLASS in 1 CARTON (72603-198-01) / 5 mL in 1 VIAL, GLASS

Annotations

UNII (FDA Substance ID)
6XC1PAD3KF
ZOLEDRONIC ACID
RxCUI 77655
Orange Book
A201783
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "6XC1PAD3KF",
    "rxcui": "77655",
    "inchikey": "FUXFIVRTGHOMSO-UHFFFAOYSA-N",
    "display_name": "ZOLEDRONIC ACID",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "1977d713-4cc7-405e-b4c1-a9a91635eff6": {
      "match": "brand_token",
      "title": "ZOLEDRONIC ACID INJECTION, SOLUTION [MYLAN INSTITUTIONAL LLC]",
      "spl_version": "6",
      "published_date": "2026-05-28"
    }
  },
  "productid": "72603-198_5499e3f9-5d5d-4eeb-a859-62cc967d468f",
  "productndc": "72603-198",
  "dosage_form": "INJECTION, SOLUTION, CONCENTRATE",
  "orange_book": {
    "appl_no": "201783",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AP",
        "strength": "EQ 4MG BASE/5ML",
        "product_no": "001",
        "approval_date": "Mar 12, 2013"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ZOLEDRONIC ACID",
  "proprietary_name": "Zoledronic acid",
  "active_ingred_unit": "mg/5mL",
  "application_number": "ANDA201783",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Zoledronic acid",
  "start_marketing_date": "20231101",
  "active_numerator_strength": "4"
}

Related drugs

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