Package 50580-533-24

Brand: benadryl allergy extra strength

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50580-533-24
Digits Only 5058053324
Product NDC 50580-533
Product ID 50580-533_21731b98-004e-db35-e063-6394a90a8397
Description

2 BLISTER PACK in 1 CARTON (50580-533-24) / 12 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2022-07-05
Brand benadryl allergy extra strength
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Benadryl Allergy EXTRA STRENGTH ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "21731b98-004e-db35-e063-6394a90a8397", "openfda": {"upc": ["0300450235244"], "unii": ["TC2D6JAD40"], "rxcui": ["1085945", "2605033"], "spl_set_id": ["dd0a8069-18d8-5696-e053-2995a90a2f22"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50580-533-24)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-533-24", "marketing_start_date": "20220705"}], "brand_name": "Benadryl Allergy EXTRA STRENGTH", "product_id": "50580-533_21731b98-004e-db35-e063-6394a90a8397", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50580-533", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl Allergy EXTRA STRENGTH", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220705", "listing_expiration_date": "20261231"}