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United States · US · US:83270-307_4972ec74-1d9b-de9b-e063-6394a90af786
oxacillin
Orange BookUNIISPLATC J01CF04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerOnesource Specialty Pharma Limited
CountryUS (United States)
ATC codeJ01CF04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11832703071010 VIAL in 1 CARTON (83270-307-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Annotations
UNII (FDA Substance ID)
G0V6C994Q5
OXACILLIN SODIUM
RxCUI 9898
Orange Book
A091486
AP
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": "INTRAMUSCULAR; 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": "83270-307_4972ec74-1d9b-de9b-e063-6394a90af786",
"productndc": "83270-307",
"dosage_form": "INJECTION, POWDER, FOR SOLUTION",
"orange_book": {
"appl_no": "091486",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 1GM BASE/VIAL",
"product_no": "001",
"approval_date": "Aug 25, 2014"
},
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 2GM BASE/VIAL",
"product_no": "002",
"approval_date": "Aug 25, 2014"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "OXACILLIN SODIUM",
"proprietary_name": "oxacillin",
"active_ingred_unit": "g/1",
"application_number": "ANDA091486",
"marketing_category": "ANDA",
"nonproprietary_name": "oxacillin",
"start_marketing_date": "20220921",
"active_numerator_strength": "2"
}Related drugs
Other records sharing ATC code J01CF04.
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