Mupirocin

Orange BookUNIISPLATC D06AX09

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

Identification

ManufacturerPAI Holdings, LLC dba PAI Pharma

CountryUS (United States)

ATC codeD06AX09

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
0121107600
100 TUBE in 1 CARTON (0121-1076-00) / 1 g in 1 TUBE (0121-1076-01)
ndc11
0121107650
50 TUBE in 1 CARTON (0121-1076-50) / 1 g in 1 TUBE (0121-1076-01)

Annotations

UNII (FDA Substance ID)

D0GX863OA5

MUPIROCIN

RxCUI 42372

Orange Book

A065170

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "D0GX863OA5",
    "rxcui": "42372",
    "inchikey": "MINDHVHHQZYEEK-HBBNESRFSA-N",
    "display_name": "MUPIROCIN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "c70dd5d7-6995-4a3d-b19c-9b4a2cfe3da9": {
      "match": "brand_token",
      "title": "MUPIROCIN OINTMENT [SPORTPHARM LLC]",
      "spl_version": "1",
      "published_date": "2026-05-13"
    }
  },
  "productid": "0121-1076_a43227b5-2dc1-40bf-a9cb-b564d480b897",
  "productndc": "0121-1076",
  "dosage_form": "OINTMENT",
  "orange_book": {
    "appl_no": "065170",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2%",
        "product_no": "001",
        "approval_date": "Sep 23, 2005"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "MUPIROCIN",
  "proprietary_name": "Mupirocin",
  "active_ingred_unit": "mg/g",
  "application_number": "ANDA065170",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Mupirocin",
  "start_marketing_date": "20260313",
  "active_numerator_strength": "20"
}

Related drugs

Other records sharing ATC code D06AX09.

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