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United States · US · US:72162-1802_338daeea-483f-25a4-e063-6294a90a5c11

Methimazole

Orange BookUNIISPLATC H03BB52

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeH03BB52
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    7216218021
    100 TABLET in 1 BOTTLE (72162-1802-1)
  • ndc11
    7216218022
    100 TABLET in 1 BOTTLE (72162-1802-2)
  • ndc11
    7216218024
    180 TABLET in 1 BOTTLE (72162-1802-4)
  • ndc11
    7216218025
    500 TABLET in 1 BOTTLE (72162-1802-5)
  • ndc11
    7216218027
    500 TABLET in 1 BOTTLE (72162-1802-7)
  • ndc11
    7216218029
    90 TABLET in 1 BOTTLE (72162-1802-9)

Annotations

UNII (FDA Substance ID)
554Z48XN5E
METHIMAZOLE
RxCUI 6835
Orange Book
A040350
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "554Z48XN5E",
    "rxcui": "6835",
    "inchikey": "PMRYVIKBURPHAH-UHFFFAOYSA-N",
    "display_name": "METHIMAZOLE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "06bb4bcc-5e47-48b6-a76c-648f846704e8": {
      "match": "brand_token",
      "title": "METHIMAZOLE TABLET [AIPING PHARMACEUTICAL, INC.]",
      "spl_version": "1",
      "published_date": "2026-04-02"
    }
  },
  "productid": "72162-1802_338daeea-483f-25a4-e063-6294a90a5c11",
  "productndc": "72162-1802",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "040350",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Mar 29, 2000"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Mar 29, 2000"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "20MG",
        "product_no": "003",
        "approval_date": "Jun 7, 2001"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "METHIMAZOLE",
  "proprietary_name": "Methimazole",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA040350",
  "marketing_category": "ANDA",
  "nonproprietary_name": "methimazole",
  "start_marketing_date": "20220314",
  "active_numerator_strength": "5"
}

Related drugs

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