Package 50580-228-49

Brand: benadryl allergy liqui-gels

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50580-228-49
Digits Only 5058022849
Product NDC 50580-228
Description

3 CARTON in 1 PACKAGE (50580-228-49) / 4 BLISTER PACK in 1 CARTON / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-06-19
Brand benadryl allergy liqui-gels
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "215d5606-66db-fa00-e063-6394a90a5c11", "openfda": {"upc": ["0312547170215"], "unii": ["TC2D6JAD40"], "rxcui": ["1049909", "1049910"], "spl_set_id": ["bfeae100-e2d1-4607-be3b-2d9b15cd4f7f"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50580-228-24)  / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "50580-228-24", "marketing_start_date": "20090301"}, {"sample": false, "description": "2 CARTON in 1 PACKAGE (50580-228-48)  / 4 BLISTER PACK in 1 CARTON / 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "50580-228-48", "marketing_start_date": "20230201"}, {"sample": false, "description": "3 CARTON in 1 PACKAGE (50580-228-49)  / 4 BLISTER PACK in 1 CARTON / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "50580-228-49", "marketing_start_date": "20230619"}], "brand_name": "Benadryl Allergy Liqui-Gels", "product_id": "50580-228_215d5606-66db-fa00-e063-6394a90a5c11", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50580-228", "generic_name": "diphenhydramine hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl Allergy Liqui-Gels", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20090301", "listing_expiration_date": "20261231"}