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United States · US · US:0093-3123_1976304d-7c32-40f7-9724-0d1903dad50e
Dicloxacillin Sodium
Orange BookUNIISPLATC J01CF01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTeva Pharmaceuticals USA, Inc.
CountryUS (United States)
ATC codeJ01CF01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110093312301100 CAPSULE in 1 BOTTLE (0093-3123-01)
Annotations
UNII (FDA Substance ID)
4HZT2V9KX0
DICLOXACILLIN SODIUM
RxCUI 267257
Orange Book
A062286
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4HZT2V9KX0",
"rxcui": "267257",
"inchikey": "SIGZQNJITOWQEF-VICXVTCVSA-M",
"display_name": "DICLOXACILLIN SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c17cd62d-ff5d-47ba-8673-3346c7f2365f": {
"match": "brand_token",
"title": "DICLOXACILLIN SODIUM CAPSULE [PD-RX PHARMACEUTICALS, INC.]",
"spl_version": "22",
"published_date": "2026-05-25"
}
},
"productid": "0093-3123_1976304d-7c32-40f7-9724-0d1903dad50e",
"productndc": "0093-3123",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "062286",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 250MG BASE",
"product_no": "001",
"approval_date": "Jun 3, 1982"
},
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "EQ 500MG BASE",
"product_no": "002",
"approval_date": "Jun 3, 1982"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DICLOXACILLIN SODIUM",
"proprietary_name": "Dicloxacillin Sodium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA062286",
"marketing_category": "ANDA",
"nonproprietary_name": "Dicloxacillin Sodium",
"start_marketing_date": "19900930",
"active_numerator_strength": "250"
}Related drugs
Other records sharing ATC code J01CF01.
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