Package 79903-053-10
Brand: extra strength pain reliever pm
Generic: acetaminophen and diphenhydramine hydrochloridePackage 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
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"}