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United States · US · US:64679-700_41e474af-6d03-f358-e063-6294a90af8e3
Oxacillin
Orange BookUNIISPLATC J01CF04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWockhardt USA LLC.
CountryUS (United States)
ATC codeJ01CF04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1164679700031 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (64679-700-03) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (64679-700-02)
Annotations
UNII (FDA Substance ID)
G0V6C994Q5
OXACILLIN SODIUM
RxCUI 9898
Orange Book
A207148
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": "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": "64679-700_41e474af-6d03-f358-e063-6294a90af8e3",
"productndc": "64679-700",
"dosage_form": "INJECTION, POWDER, FOR SOLUTION",
"orange_book": {
"appl_no": "207148",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 10GM BASE/VIAL",
"product_no": "001",
"approval_date": "Nov 24, 2017"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "OXACILLIN SODIUM",
"proprietary_name": "Oxacillin",
"active_ingred_unit": "g/100mL",
"application_number": "ANDA207148",
"marketing_category": "ANDA",
"nonproprietary_name": "Oxacillin",
"start_marketing_date": "20171124",
"active_numerator_strength": "10"
}Related drugs
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