Package 50580-370-01

Brand: benadryl

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50580-370-01
Digits Only 5058037001
Product NDC 50580-370
Description

1 KIT in 1 PACKAGE (50580-370-01) * 1 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE * 4 BLISTER PACK in 1 CARTON / 12 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2017-06-12
Brand benadryl
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "21716a1f-3636-bdde-e063-6394a90aab01", "openfda": {"rxcui": ["1049630", "1049632"], "spl_set_id": ["2884d2dc-2d4a-4ca6-ab73-688a80b428eb"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE (50580-370-01)  *  1 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE *  4 BLISTER PACK in 1 CARTON / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-370-01", "marketing_start_date": "20170612"}], "brand_name": "Benadryl", "product_id": "50580-370_21716a1f-3636-bdde-e063-6394a90aab01", "dosage_form": "KIT", "product_ndc": "50580-370", "generic_name": "diphenhydramine hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170612", "listing_expiration_date": "20261231"}