Package 70000-0411-1
Brand: acetaminophen, diphenhydramine hydrochloride
Generic: acetaminophen, diphenhydramine hydrochloridePackage Facts
Identity
Package NDC
70000-0411-1
Digits Only
7000004111
Product NDC
70000-0411
Description
1 BOTTLE in 1 CARTON (70000-0411-1) / 24 TABLET, FILM COATED in 1 BOTTLE
Marketing
Marketing Status
Brand
acetaminophen, diphenhydramine hydrochloride
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": "4bbe57b4-c0c6-c37f-e063-6294a90a7dd7", "openfda": {"upc": ["0096295135299"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["7be4d67e-1af9-f059-e053-2991aa0a382e"], "manufacturer_name": ["LEADER/ Cardinal Health 110, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0411-1) / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "70000-0411-1", "marketing_start_date": "20181210"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (70000-0411-2)", "package_ndc": "70000-0411-2", "marketing_start_date": "20181129"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0411-3) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "70000-0411-3", "marketing_start_date": "20181210"}], "brand_name": "Acetaminophen, Diphenhydramine Hydrochloride", "product_id": "70000-0411_4bbe57b4-c0c6-c37f-e063-6294a90a7dd7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70000-0411", "generic_name": "Acetaminophen, Diphenhydramine Hydrochloride", "labeler_name": "LEADER/ Cardinal Health 110, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen, Diphenhydramine Hydrochloride", "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": "20181129", "listing_expiration_date": "20271231"}