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United States · US · US:0338-1015_dc761dcc-7333-4b1c-90be-e9ec96e7b2aa
OXACILLIN
Orange BookUNIISPLATC J01CF04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBaxter Healthcare Corporation
CountryUS (United States)
ATC codeJ01CF04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11033810154150 mL in 1 BAG (0338-1015-41)
Annotations
UNII (FDA Substance ID)
G0V6C994Q5
OXACILLIN SODIUM
RxCUI 9898
Orange Book
N050640
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "G0V6C994Q5",
"rxcui": "9898",
"inchikey": "ZVIYWUUZWWBNMB-VICXVTCVSA-M",
"display_name": "OXACILLIN SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"4972ec74-1d9a-de9b-e063-6394a90af786": {
"match": "brand_token",
"title": "OXACILLIN INJECTION, POWDER, FOR SOLUTION [ONESOURCE SPECIALTY PHARMA LIMITED]",
"spl_version": "1",
"published_date": "2026-01-29"
}
},
"productid": "0338-1015_dc761dcc-7333-4b1c-90be-e9ec96e7b2aa",
"productndc": "0338-1015",
"dosage_form": "INJECTION, SOLUTION",
"orange_book": {
"appl_no": "050640",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "EQ 20MG BASE/ML",
"product_no": "001",
"approval_date": "Oct 26, 1989"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "EQ 40MG BASE/ML",
"product_no": "002",
"approval_date": "Oct 26, 1989"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "OXACILLIN SODIUM",
"proprietary_name": "OXACILLIN",
"active_ingred_unit": "g/50mL",
"application_number": "NDA050640",
"marketing_category": "NDA",
"nonproprietary_name": "OXACILLIN",
"start_marketing_date": "19891026",
"active_numerator_strength": "2"
}Related drugs
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