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United States · US · US:25021-111_79813968-4f6f-49a9-9a94-18607a1bcfbf
Cefoxitin
Orange BookUNIISPLATC J01DC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSagent Pharmaceuticals
CountryUS (United States)
ATC codeJ01DC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11250211119910 BOTTLE in 1 CARTON (25021-111-99) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
Q68050H03T
CEFOXITIN SODIUM
RxCUI 203118
Orange Book
A065415
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "Q68050H03T",
"rxcui": "203118",
"inchikey": "GNWUOVJNSFPWDD-XMZRARIVSA-M",
"display_name": "CEFOXITIN SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"91ac4c14-8dd8-4efe-a462-d1c488a6184f": {
"match": "brand_token",
"title": "CEFOXITIN INJECTION, POWDER, FOR SOLUTION [WG CRITICAL CARE, LLC]",
"spl_version": "7",
"published_date": "2025-11-17"
}
},
"productid": "25021-111_79813968-4f6f-49a9-9a94-18607a1bcfbf",
"productndc": "25021-111",
"dosage_form": "INJECTION, POWDER, FOR SOLUTION",
"orange_book": {
"appl_no": "065415",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AP",
"strength": "EQ 10GM BASE/VIAL",
"product_no": "001",
"approval_date": "May 19, 2010"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CEFOXITIN SODIUM",
"proprietary_name": "Cefoxitin",
"active_ingred_unit": "g/1",
"application_number": "ANDA065415",
"marketing_category": "ANDA",
"nonproprietary_name": "cefoxitin",
"start_marketing_date": "20100812",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code J01DC01.
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