Package 50804-825-02

Brand: pain relief pm extra strength

Generic: acetaminophen and diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50804-825-02
Digits Only 5080482502
Product NDC 50804-825
Product ID 50804-825_24c359e6-7a74-0123-e063-6394a90a0f4c
Description

1 BOTTLE, PLASTIC in 1 CARTON (50804-825-02) / 20 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2017-08-01
Brand pain relief pm extra strength
Generic acetaminophen and diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Pain Relief PM Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "24c359e6-7a74-0123-e063-6394a90a0f4c", "openfda": {"upc": ["0846036008258"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["8972d95a-51da-40b5-8ef1-9dfed220d7eb"], "manufacturer_name": ["GoodSense"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50804-825-02)  / 20 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50804-825-02", "marketing_start_date": "20170801"}], "brand_name": "Pain Relief PM Extra Strength", "product_id": "50804-825_24c359e6-7a74-0123-e063-6394a90a0f4c", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50804-825", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "GoodSense", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief PM", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170801", "listing_expiration_date": "20261231"}