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United States · US · US:60505-6244_0c841753-3bec-fb8a-e063-6294a90a0d2b
Cefazolin
Orange BookUNIISPLATC J01DB
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerApotex Corp.
CountryUS (United States)
ATC codeJ01DB
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11605056244410 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (60505-6244-4) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE (60505-6244-0)
Annotations
UNII (FDA Substance ID)
P380M0454Z
CEFAZOLIN SODIUM
RxCUI 203171
Orange Book
A209217
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "P380M0454Z",
"rxcui": "203171",
"inchikey": "FLKYBGKDCCEQQM-WYUVZMMLSA-M",
"display_name": "CEFAZOLIN SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"d91a8d13-99a0-4d87-88dc-71cbd37922b4": {
"match": "brand_token",
"title": "CEFAZOLIN (CEFAZOLIN SODIUM) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]",
"spl_version": "17",
"published_date": "2026-05-21"
}
},
"productid": "60505-6244_0c841753-3bec-fb8a-e063-6294a90a0d2b",
"productndc": "60505-6244",
"dosage_form": "INJECTION, POWDER, FOR SOLUTION",
"orange_book": {
"appl_no": "209217",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AP",
"strength": "EQ 10GM BASE/VIAL",
"product_no": "001",
"approval_date": "Oct 17, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CEFAZOLIN SODIUM",
"proprietary_name": "Cefazolin",
"active_ingred_unit": "g/1",
"application_number": "ANDA209217",
"marketing_category": "ANDA",
"nonproprietary_name": "Cefazolin",
"start_marketing_date": "20220901",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code J01DB.
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