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United States · US · US:23155-906_45e4c5b2-2a6c-481a-92c6-9ab894df195c
Nafcillin
Orange BookUNIISPLATC J01CF06
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHeritage Pharmaceuticals Inc. d/b/a/ Avet Pharmaceuticals Inc.
CountryUS (United States)
ATC codeJ01CF06
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11231559064110 VIAL in 1 CARTON (23155-906-41) / 4 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
49G3001BCK
NAFCILLIN SODIUM
RxCUI 485026
Orange Book
A090560
APAP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "49G3001BCK",
"rxcui": "485026",
"inchikey": "OCXSDHJRMYFTMA-KMFBOIRUSA-M",
"display_name": "NAFCILLIN SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAMUSCULAR; INTRAVENOUS",
"spl_meta": {
"4b3b8e52-df96-4886-e063-6294a90ac63f": {
"match": "brand_token",
"title": "NAFCILLIN SODIUM INJECTION, POWDER, FOR SOLUTION [ONESOURCE SPECIALTY PHARMA LIMITED]",
"spl_version": "2",
"published_date": "2026-04-06"
}
},
"productid": "23155-906_45e4c5b2-2a6c-481a-92c6-9ab894df195c",
"productndc": "23155-906",
"dosage_form": "INJECTION, POWDER, FOR SOLUTION",
"orange_book": {
"appl_no": "090560",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 1GM BASE/VIAL",
"product_no": "001",
"approval_date": "Oct 3, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 2GM BASE/VIAL",
"product_no": "002",
"approval_date": "Oct 3, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NAFCILLIN SODIUM",
"proprietary_name": "Nafcillin",
"active_ingred_unit": "g/4mL",
"application_number": "ANDA090560",
"marketing_category": "ANDA",
"nonproprietary_name": "Nafcillin Sodium",
"start_marketing_date": "20250131",
"active_numerator_strength": "1"
}Related drugs
Other records sharing ATC code J01CF06.
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