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United States · US · US:11673-697_18567eaf-6b97-8c6f-e063-6294a90a986d

Maximum Strength Acid Reducer

Orange BookUNIISPLATC A02BA03

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

Identification

ManufacturerTARGET CORPORATION
CountryUS (United States)
ATC codeA02BA03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    1167369701
    2 BOTTLE in 1 CARTON (11673-697-01) / 50 TABLET in 1 BOTTLE
  • ndc11
    1167369705
    1 BOTTLE in 1 CARTON (11673-697-05) / 50 TABLET in 1 BOTTLE
  • ndc11
    1167369720
    1 BOTTLE in 1 CARTON (11673-697-20) / 200 TABLET in 1 BOTTLE
  • ndc11
    1167369752
    5 BLISTER PACK in 1 CARTON (11673-697-52) / 5 TABLET in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A217543
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "5QZO15J2Z8",
    "rxcui": "4278",
    "inchikey": "XUFQPHANEAPEMJ-UHFFFAOYSA-N",
    "display_name": "FAMOTIDINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "350764de-7801-b24e-e063-6394a90ab3c3": {
      "match": "brand_token",
      "title": "MAXIMUM STRENGTH MUCINEX SINUS-MAX PRESSURE, PAIN AND COUGH (ACETAMINOPHEN, GUAIFENESIN) TABLET, FILM COATED [RECKITT BENCKISER LLC]",
      "spl_version": "2",
      "published_date": "2026-05-15"
    }
  },
  "productid": "11673-697_18567eaf-6b97-8c6f-e063-6294a90a986d",
  "productndc": "11673-697",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "217543",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Mar 8, 2023"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "20MG",
        "product_no": "002",
        "approval_date": "Mar 8, 2023"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "FAMOTIDINE",
  "proprietary_name": "Maximum Strength Acid Reducer",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA217543",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Famotidine",
  "start_marketing_date": "20240515",
  "active_numerator_strength": "20"
}

Related drugs

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