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United States · US · US:72603-453_ada50f84-5fb6-480b-a385-bb95d1181ce7
Nafcillin
Orange BookUNIISPLATC J01CF06
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNorthStar Rx, LLC
CountryUS (United States)
ATC codeJ01CF06
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1172603453011 VIAL in 1 BOX (72603-453-01) / 8 mL in 1 VIAL
- ndc11726034531010 VIAL in 1 BOX (72603-453-10) / 8 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
49G3001BCK
NAFCILLIN SODIUM
RxCUI 485026
Orange Book
A090002
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": "72603-453_ada50f84-5fb6-480b-a385-bb95d1181ce7",
"productndc": "72603-453",
"dosage_form": "INJECTION, POWDER, FOR SOLUTION",
"orange_book": {
"appl_no": "090002",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 1GM BASE/VIAL",
"product_no": "001",
"approval_date": "Jun 30, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 2GM BASE/VIAL",
"product_no": "002",
"approval_date": "Jun 30, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NAFCILLIN SODIUM",
"proprietary_name": "Nafcillin",
"active_ingred_unit": "g/8mL",
"application_number": "ANDA090002",
"marketing_category": "ANDA",
"nonproprietary_name": "Nafcillin Sodium",
"start_marketing_date": "20240701",
"active_numerator_strength": "2"
}Related drugs
Other records sharing ATC code J01CF06.
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