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United States · US · US:56062-141_edd72fec-0dfc-4862-8d07-476e74b2fe69

acid reducer

Orange BookUNIISPLATC A02BA03

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

Identification

ManufacturerPublix Super Markets Inc
CountryUS (United States)
ATC codeA02BA03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    5606214165
    30 BLISTER PACK in 1 CARTON (56062-141-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A075400
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": {
    "9826dd26-5592-4f96-9274-005ef9462cb4": {
      "match": "brand_token",
      "title": "ACID RELIEF (FAMOTIDINE) TABLET, FILM COATED [RITE AID CORPORATION]",
      "spl_version": "5",
      "published_date": "2026-05-28"
    }
  },
  "productid": "56062-141_edd72fec-0dfc-4862-8d07-476e74b2fe69",
  "productndc": "56062-141",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "075400",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Mar 18, 2005"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "FAMOTIDINE",
  "proprietary_name": "acid reducer",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA075400",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Famotidine",
  "start_marketing_date": "20091123",
  "active_numerator_strength": "10"
}

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