Package 68391-430-50

Brand: extra strength acetaminophen pm

Generic: acetaminophen, diphenhydramine
NDC Package

Package Facts

Identity

Package NDC 68391-430-50
Digits Only 6839143050
Product NDC 68391-430
Description

500 TABLET in 1 BOTTLE (68391-430-50)

Marketing

Marketing Status
Marketed Since 2025-09-01
Brand extra strength acetaminophen pm
Generic acetaminophen, diphenhydramine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3becb4c1-6d93-4349-e063-6294a90a0a52", "openfda": {"upc": ["0888670204047"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["2f473f1f-7cf3-2af5-e063-6394a90aaa17"], "manufacturer_name": ["BJWC (Berkley & Jensen / BJ's)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (68391-430-50)", "package_ndc": "68391-430-50", "marketing_start_date": "20250901"}], "brand_name": "Extra Strength Acetaminophen PM", "product_id": "68391-430_3becb4c1-6d93-4349-e063-6294a90a0a52", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68391-430", "generic_name": "Acetaminophen, Diphenhydramine", "labeler_name": "BJWC (Berkley & Jensen / BJ's)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Acetaminophen 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": "20250901", "listing_expiration_date": "20261231"}