Package 54473-304-01

Brand: counteract pm

Generic: acetaminophen and diphenhydramine
NDC Package

Package Facts

Identity

Package NDC 54473-304-01
Digits Only 5447330401
Product NDC 54473-304
Description

1 BOTTLE in 1 BOX (54473-304-01) / 50 TABLET in 1 BOTTLE (54473-304-50)

Marketing

Marketing Status
Marketed Since 2016-05-02
Brand counteract pm
Generic acetaminophen and diphenhydramine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7fbf2b51-9097-0a1f-e053-2991aa0a6aa1", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["7f9a0062-0e86-1deb-e053-2a91aa0a9188"], "manufacturer_name": ["Melaleuca, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (54473-304-01)  / 50 TABLET in 1 BOTTLE (54473-304-50)", "package_ndc": "54473-304-01", "marketing_start_date": "20160502"}], "brand_name": "CounterAct PM", "product_id": "54473-304_7fbf2b51-9097-0a1f-e053-2991aa0a6aa1", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "54473-304", "generic_name": "Acetaminophen and Diphenhydramine", "labeler_name": "Melaleuca, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CounterAct", "brand_name_suffix": "PM", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "part343", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "20160502", "listing_expiration_date": "20261231"}