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United States · US · US:73473-901_40441079-4a76-b56f-e063-6394a90a5765

Neomycin Sulfate

Orange BookUNIISPLATC R02AB01

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

Identification

ManufacturerSolaris Pharma Corporation
CountryUS (United States)
ATC codeR02AB01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7347390105
    100 TABLET in 1 BOTTLE, PLASTIC (73473-901-05)

Annotations

UNII (FDA Substance ID)
057Y626693
NEOMYCIN SULFATE
RxCUI 7300
Orange Book
A065220
AA
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "057Y626693",
    "rxcui": "7300",
    "inchikey": null,
    "display_name": "NEOMYCIN SULFATE",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "a2f47d77-efd3-4c84-a364-08fb6d9978eb": {
      "match": "brand_token",
      "title": "NEOMYCIN AND POLYMYXIN B SULFATES SOLUTION [XGEN PHARMACEUTICALS DJB, INC.]",
      "spl_version": "18",
      "published_date": "2026-05-21"
    }
  },
  "productid": "73473-901_40441079-4a76-b56f-e063-6394a90a5765",
  "productndc": "73473-901",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "065220",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "500MG",
        "product_no": "001",
        "approval_date": "Jul 28, 2006"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "NEOMYCIN SULFATE",
  "proprietary_name": "Neomycin Sulfate",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA065220",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Neomycin Sulfate",
  "start_marketing_date": "20230601",
  "active_numerator_strength": "500"
}

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