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United States · US · US:50090-2396_4c4467e1-5886-4b66-aaff-8647a8591fce

Mefloquine Hydrochloride

Orange BookUNIISPLATC P01BC02

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

Identification

ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeP01BC02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    5009023960
    1 BLISTER PACK in 1 CARTON (50090-2396-0) / 10 TABLET in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)
5Y9L3636O3
MEFLOQUINE HYDROCHLORIDE
RxCUI 82130
Orange Book
A076392
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "5Y9L3636O3",
    "rxcui": "82130",
    "inchikey": "WESWYMRNZNDGBX-YLCXCWDSSA-N;WESWYMRNZNDGBX-SBKWZQTDSA-N",
    "display_name": "MEFLOQUINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "09716a24-d7da-42b2-af29-c03a1b6670bd": {
      "match": "brand_token",
      "title": "MEFLOQUINE HYDROCHLORIDE TABLET [TEVA PHARMACEUTICALS USA, INC.]",
      "spl_version": "13",
      "published_date": "2026-02-04"
    }
  },
  "productid": "50090-2396_4c4467e1-5886-4b66-aaff-8647a8591fce",
  "productndc": "50090-2396",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "076392",
    "products": [
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "250MG",
        "product_no": "001",
        "approval_date": "Dec 29, 2003"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "MEFLOQUINE HYDROCHLORIDE",
  "proprietary_name": "Mefloquine Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA076392",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Mefloquine Hydrochloride",
  "start_marketing_date": "20040106",
  "active_numerator_strength": "250"
}

Related drugs

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