Package 79903-050-31

Brand: pain reliever pm

Generic: acetaminophen, diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 79903-050-31
Digits Only 7990305031
Product NDC 79903-050
Description

80 TABLET, COATED in 1 BOTTLE, PLASTIC (79903-050-31)

Marketing

Marketing Status
Marketed Since 2021-02-12
Brand pain reliever pm
Generic acetaminophen, diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "909846da-14d5-4f1c-8aec-4b3e6773d3cc", "openfda": {"upc": ["0681131410991"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["e50b3f60-b827-426c-8e78-8447c89130fe"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (79903-050-09)  / 20 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "79903-050-09", "marketing_start_date": "20210212"}, {"sample": false, "description": "80 TABLET, COATED in 1 BOTTLE, PLASTIC (79903-050-31)", "package_ndc": "79903-050-31", "marketing_start_date": "20210212"}], "brand_name": "Pain Reliever PM", "product_id": "79903-050_909846da-14d5-4f1c-8aec-4b3e6773d3cc", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "79903-050", "generic_name": "Acetaminophen, Diphenhydramine HCl", "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": "20210212", "listing_expiration_date": "20261231"}