Package 0615-8409-39

Brand: acetaminophen extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 0615-8409-39
Digits Only 0615840939
Product NDC 0615-8409
Product ID 0615-8409_e57e46f5-443b-469b-b046-aedeb8348034
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8409-39)

Marketing

Marketing Status
Discontinued 2026-04-30
Brand acetaminophen extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

ACETAMINOPHEN Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e57e46f5-443b-469b-b046-aedeb8348034", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["7fae4caf-a8aa-442e-97ee-0465577bdb87"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8409-30)  / 5 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0615-8409-30", "marketing_end_date": "20260331", "marketing_start_date": "20211006"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8409-39)", "package_ndc": "0615-8409-39", "marketing_end_date": "20260430", "marketing_start_date": "20211005"}], "brand_name": "ACETAMINOPHEN Extra Strength", "product_id": "0615-8409_e57e46f5-443b-469b-b046-aedeb8348034", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0615-8409", "generic_name": "ACETAMINOPHEN", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260430", "marketing_start_date": "20110718"}