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United States · US · US:64679-698_41e41b69-1cdb-60eb-e063-6394a90a1abe
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
- ndc11646796980110 VIAL in 1 CARTON (64679-698-01) / 20 mL in 1 VIAL (64679-698-02)
Annotations
UNII (FDA Substance ID)
G0V6C994Q5
OXACILLIN SODIUM
RxCUI 9898
Orange Book
A207147
APAP
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": "64679-698_41e41b69-1cdb-60eb-e063-6394a90a1abe",
"productndc": "64679-698",
"dosage_form": "INJECTION, POWDER, FOR SOLUTION",
"orange_book": {
"appl_no": "207147",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 1GM BASE/VIAL",
"product_no": "001",
"approval_date": "Jul 31, 2017"
},
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 2GM BASE/VIAL",
"product_no": "002",
"approval_date": "Jul 31, 2017"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "OXACILLIN SODIUM",
"proprietary_name": "Oxacillin",
"active_ingred_unit": "g/20mL",
"application_number": "ANDA207147",
"marketing_category": "ANDA",
"nonproprietary_name": "Oxacillin",
"start_marketing_date": "20170731",
"active_numerator_strength": "1"
}Related drugs
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