Package 79903-053-10

Brand: extra strength pain reliever pm

Generic: acetaminophen and diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 79903-053-10
Digits Only 7990305310
Product NDC 79903-053
Description

100 TABLET in 1 BOTTLE (79903-053-10)

Marketing

Marketing Status
Discontinued 2028-09-30
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": "495f38a5-3f81-52ec-e063-6394a90abef7", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["649e0dd8-ca79-4bf1-9c15-9db9f1d2f5bd"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (79903-053-10)", "package_ndc": "79903-053-10", "marketing_end_date": "20280930", "marketing_start_date": "20210113"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (79903-053-24)  / 24 TABLET in 1 BOTTLE", "package_ndc": "79903-053-24", "marketing_end_date": "20290630", "marketing_start_date": "20210113"}], "brand_name": "EXTRA STRENGTH PAIN RELIEVER PM", "product_id": "79903-053_495f38a5-3f81-52ec-e063-6394a90abef7", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "79903-053", "generic_name": "ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "WALMART INC.", "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_start_date": "20210113", "listing_expiration_date": "20271231"}