Package 62936-0201-1

Brand: extra strength pain reliever

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 62936-0201-1
Digits Only 6293602011
Product NDC 62936-0201
Description

100 TABLET in 1 BOTTLE (62936-0201-1)

Marketing

Marketing Status
Discontinued 2026-09-30
Brand extra strength pain reliever
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e8992b1-b02f-679c-e063-6394a90a2748", "openfda": {"upc": ["0086854012024"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["10e4bbe2-a47e-ff16-e063-6294a90a56a1"], "manufacturer_name": ["INGLES MARKETS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62936-0201-1)", "package_ndc": "62936-0201-1", "marketing_end_date": "20260930", "marketing_start_date": "20190101"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (62936-0201-6)", "package_ndc": "62936-0201-6", "marketing_end_date": "20260930", "marketing_start_date": "20190101"}], "brand_name": "Extra Strength Pain Reliever", "product_id": "62936-0201_3e8992b1-b02f-679c-e063-6394a90a2748", "dosage_form": "TABLET", "product_ndc": "62936-0201", "generic_name": "Acetaminophen", "labeler_name": "INGLES MARKETS, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Pain Reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260930", "marketing_start_date": "20060101"}