Package 0067-8137-20

Brand: theraflu expressmax nighttime severe cold and cough

Generic: acetaminophen, diphenhydramine hcl, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 0067-8137-20
Digits Only 0067813720
Product NDC 0067-8137
Description

2 BLISTER PACK in 1 CARTON (0067-8137-20) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2016-07-05
Brand theraflu expressmax nighttime severe cold and cough
Generic acetaminophen, diphenhydramine hcl, phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "13185fea-1e12-cf5a-e063-6394a90a18af", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1233575"], "spl_set_id": ["62f7fcb9-e31a-4634-b1c2-44a9567e3a61"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0067-8137-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0067-8137-10", "marketing_start_date": "20170608"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0067-8137-20)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0067-8137-20", "marketing_start_date": "20160705"}], "brand_name": "Theraflu ExpressMax Nighttime Severe Cold and Cough", "product_id": "0067-8137_13185fea-1e12-cf5a-e063-6394a90a18af", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0067-8137", "generic_name": "acetaminophen, diphenhydramine HCl, phenylephrine HCl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu ExpressMax", "brand_name_suffix": "Nighttime Severe Cold and Cough", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "12.5 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160705", "listing_expiration_date": "20261231"}