Package 79903-298-10
Brand: pain reliever pm
Generic: acetaminophen, diphenhydramine hydrochloridePackage Facts
Identity
Package NDC
79903-298-10
Digits Only
7990329810
Product NDC
79903-298
Description
100 TABLET in 1 BOTTLE (79903-298-10)
Marketing
Marketing Status
Brand
pain reliever pm
Generic
acetaminophen, diphenhydramine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ac07bee-6fd6-0b68-e063-6294a90a328a", "openfda": {"upc": ["0194346377107"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["21ab3d58-bb0e-3e51-e063-6294a90ad415"], "manufacturer_name": ["Walmart Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (79903-298-10)", "package_ndc": "79903-298-10", "marketing_start_date": "20250115"}], "brand_name": "Pain Reliever PM", "product_id": "79903-298_3ac07bee-6fd6-0b68-e063-6294a90a328a", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "79903-298", "generic_name": "Acetaminophen, Diphenhydramine Hydrochloride", "labeler_name": "Walmart Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "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_start_date": "20250115", "listing_expiration_date": "20261231"}