Package 53209-1001-2

Brand: tylenol extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 53209-1001-2
Digits Only 5320910012
Product NDC 53209-1001
Product ID 53209-1001_37e8d749-91bb-a5bc-e063-6394a90ac8a8
Description

25 BLISTER PACK in 1 POUCH (53209-1001-2) / 2 TABLET, FILM COATED in 1 BLISTER PACK (53209-1001-1)

Marketing

Marketing Status
Marketed Since 2025-06-19
Brand tylenol extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

TYLENOL Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "37e8d749-91bb-a5bc-e063-6394a90ac8a8", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440", "209459"], "spl_set_id": ["8502ea21-937d-4b33-a3e0-ffab5dc38cd8"], "manufacturer_name": ["Morning Star OTC"]}, "finished": true, "packaging": [{"sample": false, "description": "25 BLISTER PACK in 1 POUCH (53209-1001-2)  / 2 TABLET, FILM COATED in 1 BLISTER PACK (53209-1001-1)", "package_ndc": "53209-1001-2", "marketing_start_date": "20250619"}], "brand_name": "TYLENOL Extra Strength", "product_id": "53209-1001_37e8d749-91bb-a5bc-e063-6394a90ac8a8", "dosage_form": "TABLET, FILM COATED", "product_ndc": "53209-1001", "generic_name": "Acetaminophen", "labeler_name": "Morning Star OTC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TYLENOL Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19840819", "listing_expiration_date": "20261231"}