Package 41250-195-03

Brand: pain relief pm

Generic: acetaminophen and diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 41250-195-03
Digits Only 4125019503
Product NDC 41250-195
Description

1 BOTTLE, PLASTIC in 1 CARTON (41250-195-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-09-30
Brand pain relief pm
Generic acetaminophen and diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "243471b8-1836-664c-e063-6294a90abce7", "openfda": {"upc": ["0708820130104"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["8504a0ea-b020-58ba-e053-2a91aa0a81a8"], "manufacturer_name": ["Meijer"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (41250-195-02)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "41250-195-02", "marketing_end_date": "20260930", "marketing_start_date": "20170501"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (41250-195-03)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "41250-195-03", "marketing_end_date": "20260930", "marketing_start_date": "20170501"}, {"sample": false, "description": "2 BOTTLE, PLASTIC in 1 CARTON (41250-195-09)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "41250-195-09", "marketing_end_date": "20260930", "marketing_start_date": "20170501"}], "brand_name": "pain relief PM", "product_id": "41250-195_243471b8-1836-664c-e063-6294a90abce7", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "41250-195", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "Meijer", "product_type": "HUMAN OTC DRUG", "brand_name_base": "pain relief PM", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260930", "marketing_start_date": "20170501"}