Package 0067-8139-02
Brand: excedrin tension headache
Generic: acetaminophen, caffeinePackage Facts
Identity
Package NDC
0067-8139-02
Digits Only
0067813902
Product NDC
0067-8139
Description
1 BOTTLE in 1 CARTON (0067-8139-02) / 100 TABLET, FILM COATED in 1 BOTTLE
Marketing
Marketing Status
Brand
excedrin tension headache
Generic
acetaminophen, caffeine
Sample Package
No
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dd87f543-c93b-4204-a601-368db2fec725", "openfda": {"nui": ["N0000175739", "N0000175729", "N0000175790", "M0023046"], "unii": ["362O9ITL9D", "3G6A5W338E"], "rxcui": ["307686", "404172"], "spl_set_id": ["12c074d1-81ac-47d2-8747-b018cda0058a"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_pe": ["Central Nervous System Stimulation [PE]"], "pharm_class_epc": ["Central Nervous System Stimulant [EPC]", "Methylxanthine [EPC]"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0067-8139-01) / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0067-8139-01", "marketing_start_date": "20161215"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0067-8139-02) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0067-8139-02", "marketing_start_date": "20161215"}], "brand_name": "Excedrin Tension Headache", "product_id": "0067-8139_dd87f543-c93b-4204-a601-368db2fec725", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "0067-8139", "generic_name": "Acetaminophen, Caffeine", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Excedrin", "brand_name_suffix": "Tension Headache", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "CAFFEINE", "strength": "65 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20161215", "listing_expiration_date": "20261231"}