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United States · US · US:0555-0171_4b2b45f8-ed63-4b3c-87c5-801996f5b154

Mefloquine Hydrochloride

Orange BookUNIISPLATC P01BC02

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

Identification

ManufacturerTeva Pharmaceuticals USA, Inc.
CountryUS (United States)
ATC codeP01BC02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0555017178
    25 BLISTER PACK in 1 CARTON (0555-0171-78) / 1 TABLET in 1 BLISTER PACK (0555-0171-88)

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": "0555-0171_4b2b45f8-ed63-4b3c-87c5-801996f5b154",
  "productndc": "0555-0171",
  "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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