Package 0067-8148-01

Brand: excedrin pm triple action caplets and excedrin extra strength pain reliever

Generic: acetaminophen, aspirin (nsaid), caffeine, and diphenhydramine citrate
NDC Package

Package Facts

Identity

Package NDC 0067-8148-01
Digits Only 0067814801
Product NDC 0067-8148
Product ID 0067-8148_4b80de14-ddcc-e314-e063-6394a90aaa0f
Description

1 KIT in 1 PACKAGE, COMBINATION (0067-8148-01) * 1 BOTTLE in 1 CARTON (0067-2056-24) / 24 TABLET, COATED in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0067-2000-91) / 100 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-05-01
Brand excedrin pm triple action caplets and excedrin extra strength pain reliever
Generic acetaminophen, aspirin (nsaid), caffeine, and diphenhydramine citrate
Sample Package No

Linked Drug Pages (1)

Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "4b80de14-ddcc-e314-e063-6394a90aaa0f", "openfda": {"rxcui": ["209468", "308297", "1593110", "1593116", "2047427", "2047428"], "spl_set_id": ["444fa225-c204-45d1-b3b3-aa5650ee5d07"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE, COMBINATION (0067-8148-01)  *  1 BOTTLE in 1 CARTON (0067-2056-24)  / 24 TABLET, COATED in 1 BOTTLE *  1 BOTTLE in 1 CARTON (0067-2000-91)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0067-8148-01", "marketing_start_date": "20180501"}], "brand_name": "Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever", "product_id": "0067-8148_4b80de14-ddcc-e314-e063-6394a90aaa0f", "dosage_form": "KIT", "product_ndc": "0067-8148", "generic_name": "Acetaminophen, Aspirin (NSAID), Caffeine, and Diphenhydramine Citrate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever", "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180501", "listing_expiration_date": "20271231"}