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United States · US · US:71205-276_38e967e3-f465-48f7-9a0f-ac32a52d6c78

Famotidine

Orange BookUNIISPLATC A02BA03

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

Identification

ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeA02BA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 7

  • ndc11
    7120527606
    6 TABLET, FILM COATED in 1 BOTTLE (71205-276-06)
  • ndc11
    7120527610
    10 TABLET, FILM COATED in 1 BOTTLE (71205-276-10)
  • ndc11
    7120527630
    30 TABLET, FILM COATED in 1 BOTTLE (71205-276-30)
  • ndc11
    7120527660
    60 TABLET, FILM COATED in 1 BOTTLE (71205-276-60)
  • ndc11
    7120527667
    270 TABLET, FILM COATED in 1 BOTTLE (71205-276-67)
  • ndc11
    7120527678
    180 TABLET, FILM COATED in 1 BOTTLE (71205-276-78)
  • ndc11
    7120527690
    90 TABLET, FILM COATED in 1 BOTTLE (71205-276-90)

Annotations

UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A075511
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": "71205-276_38e967e3-f465-48f7-9a0f-ac32a52d6c78",
  "productndc": "71205-276",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "075511",
    "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": "ANDA075511",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Famotidine",
  "start_marketing_date": "20010416",
  "active_numerator_strength": "20"
}

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