Package 21130-492-01

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 21130-492-01
Digits Only 2113049201
Product NDC 21130-492
Product ID 21130-492_284fb7b3-5211-ebf1-e063-6394a90a0450
Description

1 BOTTLE, PLASTIC in 1 CARTON (21130-492-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2022-06-10
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": "284fb7b3-5211-ebf1-e063-6394a90a0450", "openfda": {"upc": ["0321130181293"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["d2d15e06-e9eb-3d2b-e053-2995a90a1cec"], "manufacturer_name": ["SAFEWAY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (21130-492-01)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "21130-492-01", "marketing_start_date": "20220610"}], "brand_name": "Pain Relief Extra Strength", "product_id": "21130-492_284fb7b3-5211-ebf1-e063-6394a90a0450", "dosage_form": "TABLET, COATED", "product_ndc": "21130-492", "generic_name": "Acetaminophen", "labeler_name": "SAFEWAY", "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": "20220610", "listing_expiration_date": "20261231"}