Package 0363-9085-15

Brand: extra strength pain reliever pm

Generic: acetaminophen and diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0363-9085-15
Digits Only 0363908515
Product NDC 0363-9085
Description

1 BOTTLE in 1 CARTON (0363-9085-15) / 15 TABLET in 1 BOTTLE

Marketing

Marketing Status
Discontinued 2028-11-30
Brand extra strength pain reliever 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": "48d64463-5a70-6a97-e063-6294a90a6bd2", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["5a58d620-a0ec-48d7-92dd-3f3f78ec10ea"], "manufacturer_name": ["WALGREENS CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-9085-15)  / 15 TABLET in 1 BOTTLE", "package_ndc": "0363-9085-15", "marketing_end_date": "20281130", "marketing_start_date": "20230413"}], "brand_name": "EXTRA STRENGTH PAIN RELIEVER PM", "product_id": "0363-9085_48d64463-5a70-6a97-e063-6294a90a6bd2", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-9085", "generic_name": "ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "WALGREENS CO.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "EXTRA STRENGTH PAIN RELIEVER 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": "20281130", "marketing_start_date": "20230413"}