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United States · US · US:71335-1950_6e3954f4-f887-4ead-9790-c5262ccf5307

Famotidine

Orange BookUNIISPLATC A02BA03

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeA02BA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7133519500
    40 TABLET, FILM COATED in 1 BOTTLE (71335-1950-0)
  • ndc11
    7133519501
    30 TABLET, FILM COATED in 1 BOTTLE (71335-1950-1)
  • ndc11
    7133519502
    60 TABLET, FILM COATED in 1 BOTTLE (71335-1950-2)
  • ndc11
    7133519503
    20 TABLET, FILM COATED in 1 BOTTLE (71335-1950-3)
  • ndc11
    7133519504
    90 TABLET, FILM COATED in 1 BOTTLE (71335-1950-4)
  • ndc11
    7133519505
    100 TABLET, FILM COATED in 1 BOTTLE (71335-1950-5)
  • ndc11
    7133519506
    10 TABLET, FILM COATED in 1 BOTTLE (71335-1950-6)
  • ndc11
    7133519507
    120 TABLET, FILM COATED in 1 BOTTLE (71335-1950-7)
  • ndc11
    7133519508
    50 TABLET, FILM COATED in 1 BOTTLE (71335-1950-8)
  • ndc11
    7133519509
    14 TABLET, FILM COATED in 1 BOTTLE (71335-1950-9)

Annotations

UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A075718
ABAB
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": "71335-1950_6e3954f4-f887-4ead-9790-c5262ccf5307",
  "productndc": "71335-1950",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "075718",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "001",
        "approval_date": "Apr 16, 2001"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "002",
        "approval_date": "Apr 16, 2001"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "FAMOTIDINE",
  "proprietary_name": "Famotidine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA075718",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Famotidine",
  "start_marketing_date": "20010416",
  "active_numerator_strength": "20"
}

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