Package 55910-812-32

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 55910-812-32
Digits Only 5591081232
Product NDC 55910-812
Product ID 55910-812_ff0f7223-4a62-4f38-99d0-d108f13a8e9a
Description

120 TABLET, COATED in 1 BOTTLE, PLASTIC (55910-812-32)

Marketing

Marketing Status
Marketed Since 2004-05-10
Brand pain relief extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Pain Relief Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ff0f7223-4a62-4f38-99d0-d108f13a8e9a", "openfda": {"upc": ["0350844519320"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["ce9f4e0d-43fb-499a-b8a2-a997a14841c4"], "manufacturer_name": ["DOLGENCORP, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, COATED in 1 BOTTLE, PLASTIC (55910-812-32)", "package_ndc": "55910-812-32", "marketing_start_date": "20040510"}], "brand_name": "Pain Relief Extra Strength", "product_id": "55910-812_ff0f7223-4a62-4f38-99d0-d108f13a8e9a", "dosage_form": "TABLET, COATED", "product_ndc": "55910-812", "generic_name": "Acetaminophen", "labeler_name": "DOLGENCORP, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20040510", "listing_expiration_date": "20261231"}