Package 37808-792-03

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 37808-792-03
Digits Only 3780879203
Product NDC 37808-792
Product ID 37808-792_24fec5b0-65f6-5e20-e063-6394a90a66bc
Description

1 BOTTLE, PLASTIC in 1 CARTON (37808-792-03) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2013-02-01
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": "24fec5b0-65f6-5e20-e063-6394a90a66bc", "openfda": {"upc": ["0041220278589"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["0863aeaa-15ec-4c67-ba79-4dad54555bd2"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (37808-792-01)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "37808-792-01", "marketing_start_date": "20130201"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (37808-792-03)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "37808-792-03", "marketing_start_date": "20130201"}], "brand_name": "Pain Relief Extra Strength", "product_id": "37808-792_24fec5b0-65f6-5e20-e063-6394a90a66bc", "dosage_form": "TABLET, COATED", "product_ndc": "37808-792", "generic_name": "Acetaminophen", "labeler_name": "HEB", "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": "20130201", "listing_expiration_date": "20261231"}