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United States · US · US:31722-023_4998217b-01c6-d647-e063-6294a90a2ff9

Oxcarbazepine

Orange BookUNIISPLATC N03AF02

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerCamber Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeN03AF02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    3172202301
    100 TABLET, FILM COATED in 1 BOTTLE (31722-023-01)
  • ndc11
    3172202305
    500 TABLET, FILM COATED in 1 BOTTLE (31722-023-05)
  • ndc11
    3172202310
    1000 TABLET, FILM COATED in 1 BOTTLE (31722-023-10)
  • ndc11
    3172202331
    10 BLISTER PACK in 1 CARTON (31722-023-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)
VZI5B1W380
OXCARBAZEPINE
RxCUI 32624
Orange Book
A215939
ABABAB
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": "31722-023_4998217b-01c6-d647-e063-6294a90a2ff9",
  "productndc": "31722-023",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "215939",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "150MG",
        "product_no": "001",
        "approval_date": "Jan 11, 2022"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "300MG",
        "product_no": "002",
        "approval_date": "Jan 11, 2022"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "600MG",
        "product_no": "003",
        "approval_date": "Jan 11, 2022"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "OXCARBAZEPINE",
  "proprietary_name": "Oxcarbazepine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA215939",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Oxcarbazepine",
  "start_marketing_date": "20220111",
  "active_numerator_strength": "150"
}

Related drugs

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