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United States · US · US:0264-3123_0cca0e6a-3047-4142-af33-d9b98efe85b1
Cefoxitin and Dextrose
Orange BookUNIISPLATC J01DC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerB. Braun Medical Inc.
CountryUS (United States)
ATC codeJ01DC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11026431231124 CONTAINER in 1 CASE (0264-3123-11) / 50 mL in 1 CONTAINER
Annotations
UNII (FDA Substance ID)
Q68050H03T
CEFOXITIN SODIUM
RxCUI 203118
Orange Book
N065214
APAP
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": "0264-3123_0cca0e6a-3047-4142-af33-d9b98efe85b1",
"productndc": "0264-3123",
"dosage_form": "INJECTION, SOLUTION",
"orange_book": {
"appl_no": "065214",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AP",
"strength": "EQ 1GM BASE/VIAL",
"product_no": "001",
"approval_date": "Mar 10, 2006"
},
{
"rs": true,
"rld": true,
"te_code": "AP",
"strength": "EQ 2GM BASE/VIAL",
"product_no": "002",
"approval_date": "Mar 10, 2006"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CEFOXITIN SODIUM",
"proprietary_name": "Cefoxitin and Dextrose",
"active_ingred_unit": "g/50mL",
"application_number": "NDA065214",
"marketing_category": "NDA",
"nonproprietary_name": "CEFOXITIN SODIUM",
"start_marketing_date": "20060310",
"active_numerator_strength": "1"
}Related drugs
Other records sharing ATC code J01DC01.
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