Package 56062-437-71

Brand: pain relief pm extra strength

Generic: acetaminophen, diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 56062-437-71
Digits Only 5606243771
Product NDC 56062-437
Description

1 BOTTLE in 1 CARTON (56062-437-71) / 50 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 1993-09-22
Brand pain relief pm extra strength
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": "30a3e4c3-88bf-4126-80ff-f63f50e90ba1", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["42d271b7-b45f-4497-8de2-4e05b4bebfa9"], "manufacturer_name": ["Publix Super Markets Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-437-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-437-71", "marketing_start_date": "19930922"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-437-78)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-437-78", "marketing_start_date": "19930922"}], "brand_name": "pain relief pm extra strength", "product_id": "56062-437_30a3e4c3-88bf-4126-80ff-f63f50e90ba1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "56062-437", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "Publix Super Markets Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "pain relief pm", "brand_name_suffix": "extra strength", "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": "19930922", "listing_expiration_date": "20261231"}