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United States · US · US:44567-246_fa6d5377-af57-45a8-aa38-685877c809a7
Cefoxitin
Orange BookUNIISPLATC J01DC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWG Critical Care, LLC
CountryUS (United States)
ATC codeJ01DC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11445672462525 VIAL in 1 CARTON (44567-246-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Annotations
UNII (FDA Substance ID)
Q68050H03T
CEFOXITIN SODIUM
RxCUI 203118
Orange Book
A065414
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": "44567-246_fa6d5377-af57-45a8-aa38-685877c809a7",
"productndc": "44567-246",
"dosage_form": "INJECTION, POWDER, FOR SOLUTION",
"orange_book": {
"appl_no": "065414",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AP",
"strength": "EQ 1GM BASE/VIAL",
"product_no": "001",
"approval_date": "Jun 12, 2009"
},
{
"rs": true,
"rld": false,
"te_code": "AP",
"strength": "EQ 2GM BASE/VIAL",
"product_no": "002",
"approval_date": "Jun 12, 2009"
}
],
"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": "ANDA065414",
"marketing_category": "ANDA",
"nonproprietary_name": "Cefoxitin",
"start_marketing_date": "20150218",
"active_numerator_strength": "2"
}Related drugs
Other records sharing ATC code J01DC01.
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