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United States · US · US:70860-119_2cc9cc61-54ac-9a94-e063-6394a90a2376

Nafcillin

Orange BookUNIISPLATC J01CF06

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

Identification

ManufacturerAthenex Pharmaceutical Division, LLC.
CountryUS (United States)
ATC codeJ01CF06
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7086011999
    1 BOTTLE in 1 CARTON (70860-119-99) / 100 mL in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
49G3001BCK
NAFCILLIN SODIUM
RxCUI 485026
Orange Book
A090005
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "49G3001BCK",
    "rxcui": "485026",
    "inchikey": "OCXSDHJRMYFTMA-KMFBOIRUSA-M",
    "display_name": "NAFCILLIN SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "4b3b8e52-df96-4886-e063-6294a90ac63f": {
      "match": "brand_token",
      "title": "NAFCILLIN SODIUM INJECTION, POWDER, FOR SOLUTION [ONESOURCE SPECIALTY PHARMA LIMITED]",
      "spl_version": "2",
      "published_date": "2026-04-06"
    }
  },
  "productid": "70860-119_2cc9cc61-54ac-9a94-e063-6394a90a2376",
  "productndc": "70860-119",
  "dosage_form": "INJECTION, POWDER, FOR SOLUTION",
  "orange_book": {
    "appl_no": "090005",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AP",
        "strength": "EQ 10GM BASE/VIAL",
        "product_no": "001",
        "approval_date": "Apr 20, 2011"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "NAFCILLIN SODIUM",
  "proprietary_name": "Nafcillin",
  "active_ingred_unit": "g/100mL",
  "application_number": "ANDA090005",
  "marketing_category": "ANDA",
  "nonproprietary_name": "nafcillin sodium",
  "start_marketing_date": "20180815",
  "active_numerator_strength": "10"
}

Related drugs

Other records sharing ATC code J01CF06.

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