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United States · US · US:50742-239_64851116-6653-4b86-9bc0-24f93b4ece10

MEXILETINE HYDROCHLORIDE

Orange BookUNIISPLATC C01BB02

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

Identification

ManufacturerIngenus Pharmaceuticals, LLC
CountryUS (United States)
ATC codeC01BB02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    5074223901
    100 CAPSULE in 1 BOTTLE (50742-239-01)

Annotations

UNII (FDA Substance ID)
606D60IS38
MEXILETINE HYDROCHLORIDE
RxCUI 142138
Orange Book
A214352
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "606D60IS38",
    "rxcui": "142138",
    "inchikey": "NFEIBWMZVIVJLQ-UHFFFAOYSA-N",
    "display_name": "MEXILETINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "a61a07f6-0b48-4dcd-ad42-5d90f6e69ab1": {
      "match": "brand_token",
      "title": "MEXILETINE HYDROCHLORIDE CAPSULE [MACLEODS PHARMACEUTICALS LIMITED]",
      "spl_version": "1",
      "published_date": "2026-04-17"
    }
  },
  "productid": "50742-239_64851116-6653-4b86-9bc0-24f93b4ece10",
  "productndc": "50742-239",
  "dosage_form": "CAPSULE",
  "orange_book": {
    "appl_no": "214352",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "150MG",
        "product_no": "001",
        "approval_date": "Jan 25, 2021"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "200MG",
        "product_no": "002",
        "approval_date": "Jan 25, 2021"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "250MG",
        "product_no": "003",
        "approval_date": "Jan 25, 2021"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "MEXILETINE HYDROCHLORIDE",
  "proprietary_name": "MEXILETINE HYDROCHLORIDE",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA214352",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Mexiletine hydrochloride",
  "start_marketing_date": "20210126",
  "active_numerator_strength": "150"
}

Related drugs

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