benadryl ultra tab

Generic: diphenhydramine hydrochloride

Labeler: jc world bell wholesale co., inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name benadryl ultra tab
Generic Name diphenhydramine hydrochloride
Labeler jc world bell wholesale co., inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

diphenhydramine hydrochloride 25 mg/1

Manufacturer
JC World Bell Wholesale Co., Inc.

Identifiers & Regulatory

Product NDC 50269-226
Product ID 50269-226_2a95607f-55a6-2f9a-e063-6394a90ac2db
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2018-08-16

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50269226
Hyphenated Format 50269-226

Supplemental Identifiers

RxCUI
1049630 1049632
UPC
0852682507663
UNII
TC2D6JAD40

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name benadryl ultra tab (source: ndc)
Generic Name diphenhydramine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 25 TABLET, FILM COATED in 1 BOX (50269-226-54)
source: ndc

Packages (1)

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

Ingredients (1)

diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Benadryl Ultra Tab ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a95607f-55a6-2f9a-e063-6394a90ac2db", "openfda": {"upc": ["0852682507663"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630", "1049632"], "spl_set_id": ["17633c87-ff0f-4fde-ab23-bc43bdc3fa8e"], "manufacturer_name": ["JC World Bell Wholesale Co., Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "25 TABLET, FILM COATED in 1 BOX (50269-226-54)", "package_ndc": "50269-226-54", "marketing_start_date": "20180816"}], "brand_name": "Benadryl Ultra Tab", "product_id": "50269-226_2a95607f-55a6-2f9a-e063-6394a90ac2db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50269-226", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "JC World Bell Wholesale Co., Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl Ultra Tab", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180816", "listing_expiration_date": "20261231"}