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United States · US · US:0143-9876_3de36693-e566-4f2a-b9fe-8b777b275fa4
Cefoxitin
Orange BookUNIISPLATC J01DC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHikma Pharmaceuticals USA Inc.
CountryUS (United States)
ATC codeJ01DC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11014398761010 BOTTLE in 1 CARTON (0143-9876-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE (0143-9876-01)
Annotations
UNII (FDA Substance ID)
Q68050H03T
CEFOXITIN SODIUM
RxCUI 203118
Orange Book
A065239
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": "0143-9876_3de36693-e566-4f2a-b9fe-8b777b275fa4",
"productndc": "0143-9876",
"dosage_form": "INJECTION, POWDER, FOR SOLUTION",
"orange_book": {
"appl_no": "065239",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 10GM BASE/VIAL",
"product_no": "001",
"approval_date": "Mar 2, 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": "ANDA065239",
"marketing_category": "ANDA",
"nonproprietary_name": "Cefoxitin",
"start_marketing_date": "20100226",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code J01DC01.
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