Package 50269-226-54

Brand: benadryl ultra tab

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50269-226-54
Digits Only 5026922654
Product NDC 50269-226
Product ID 50269-226_2a95607f-55a6-2f9a-e063-6394a90ac2db
Description

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

Marketing

Marketing Status
Marketed Since 2018-08-16
Brand benadryl ultra tab
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Benadryl Ultra Tab ndc-match (0.95)

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"}