Benadryl Ultra Tab

UNIISPLATC D04AA32

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerJC World Bell Wholesale Co., Inc.

CountryUS (United States)

ATC codeD04AA32

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5026922654
25 TABLET, FILM COATED in 1 BOX (50269-226-54)

Annotations

UNII (FDA Substance ID)

TC2D6JAD40

DIPHENHYDRAMINE HYDROCHLORIDE

RxCUI 1362

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "TC2D6JAD40",
    "rxcui": "1362",
    "inchikey": "PCHPORCSPXIHLZ-UHFFFAOYSA-N",
    "display_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "8d59d121-62a8-c43b-e053-2a95a90a5847": {
      "match": "brand_token",
      "title": "BENADRYL ALLERGY ULTRATAB (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [SAVINGS DISTRIBUTORS LLC]",
      "spl_version": "3",
      "published_date": "2026-05-13"
    }
  },
  "productid": "50269-226_2a95607f-55a6-2f9a-e063-6394a90ac2db",
  "productndc": "50269-226",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
  "proprietary_name": "Benadryl Ultra Tab",
  "active_ingred_unit": "mg/1",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
  "start_marketing_date": "20180816",
  "active_numerator_strength": "25"
}

Related drugs

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