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United States · US · US:51672-1393_440646d8-f538-5968-e063-6394a90ab7cd
OXCARBAZEPINE
Orange BookUNIISPLATC N03AF02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeN03AF02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1151672139311 BOTTLE, GLASS in 1 CARTON (51672-1393-1) / 250 mL in 1 BOTTLE, GLASS
Annotations
UNII (FDA Substance ID)
VZI5B1W380
OXCARBAZEPINE
RxCUI 32624
Orange Book
A078734
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "VZI5B1W380",
"rxcui": "32624",
"inchikey": "CTRLABGOLIVAIY-UHFFFAOYSA-N",
"display_name": "OXCARBAZEPINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"a18f591b-587e-4769-8ac2-9cfba0b82526": {
"match": "brand_token",
"title": "OXCARBAZEPINE (OXCARBAZEPINE) SUSPENSION [CAMBER PHARMACEUTICALS, INC.]",
"spl_version": "3",
"published_date": "2026-05-25"
}
},
"productid": "51672-1393_440646d8-f538-5968-e063-6394a90ab7cd",
"productndc": "51672-1393",
"dosage_form": "SUSPENSION",
"orange_book": {
"appl_no": "078734",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "300MG/5ML",
"product_no": "001",
"approval_date": "Jun 26, 2009"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "OXCARBAZEPINE",
"proprietary_name": "OXCARBAZEPINE",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA078734",
"marketing_category": "ANDA",
"nonproprietary_name": "OXCARBAZEPINE",
"start_marketing_date": "20250806",
"active_numerator_strength": "60"
}Related drugs
Other records sharing ATC code N03AF02.
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