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United States · US · US:69230-327_eabd2ff8-a7d9-2ac4-e053-2995a90a3b40

famotidine

Orange BookUNIISPLATC A02BA03

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

Identification

ManufacturerCamber Consumer Care Inc
CountryUS (United States)
ATC codeA02BA03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 5

  • ndc11
    6923032701
    1 BOTTLE in 1 CARTON (69230-327-01) / 100 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    6923032705
    1 BOTTLE in 1 CARTON (69230-327-05) / 500 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    6923032710
    1 BOTTLE in 1 CARTON (69230-327-10) / 1000 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    6923032730
    1 BOTTLE in 1 CARTON (69230-327-30) / 30 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    6923032750
    1 BOTTLE in 1 CARTON (69230-327-50) / 50 TABLET, FILM COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A215766
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": {
    "e53928f3-5181-490b-acfb-be8d4cea60a9": {
      "match": "brand_token",
      "title": "FAMOTIDINE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS]",
      "spl_version": "1",
      "published_date": "2026-06-01"
    }
  },
  "productid": "69230-327_eabd2ff8-a7d9-2ac4-e053-2995a90a3b40",
  "productndc": "69230-327",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "215766",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Nov 8, 2021"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "20MG",
        "product_no": "002",
        "approval_date": "Nov 8, 2021"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "FAMOTIDINE",
  "proprietary_name": "famotidine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA215766",
  "marketing_category": "ANDA",
  "nonproprietary_name": "famotidine",
  "start_marketing_date": "20211108",
  "active_numerator_strength": "20"
}

Related drugs

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