Package 0067-2001-01
Brand: excedrin extra strength pain reliever
Generic: acetaminophen, aspirin (nsaid), and caffeinePackage Facts
Identity
Package NDC
0067-2001-01
Digits Only
0067200101
Product NDC
0067-2001
Description
2 TABLET, FILM COATED in 1 POUCH (0067-2001-01)
Marketing
Marketing Status
Brand
excedrin extra strength pain reliever
Generic
acetaminophen, aspirin (nsaid), and caffeine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "155eb367-99df-1f50-e063-6294a90a21d6", "openfda": {"nui": ["N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "unii": ["362O9ITL9D", "R16CO5Y76E", "3G6A5W338E"], "rxcui": ["209468", "308297"], "spl_set_id": ["1b5ff867-5442-4cf8-bd1e-530093cc88f8"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]", "Xanthines [CS]"], "pharm_class_pe": ["Decreased Prostaglandin Production [PE]", "Decreased Platelet Aggregation [PE]", "Central Nervous System Stimulation [PE]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]", "Central Nervous System Stimulant [EPC]", "Methylxanthine [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 POUCH (0067-2001-01)", "package_ndc": "0067-2001-01", "marketing_start_date": "20210131"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0067-2001-02) / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0067-2001-02", "marketing_start_date": "20200930"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0067-2001-03) / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0067-2001-03", "marketing_start_date": "20200930"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0067-2001-04) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0067-2001-04", "marketing_start_date": "20200930"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0067-2001-05) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0067-2001-05", "marketing_start_date": "20190315"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0067-2001-06) / 125 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0067-2001-06", "marketing_start_date": "20200930"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0067-2001-07) / 200 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0067-2001-07", "marketing_start_date": "20200930"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0067-2001-08) / 300 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0067-2001-08", "marketing_start_date": "20190315"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0067-2001-09) / 250 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0067-2001-09", "marketing_start_date": "20200930"}, {"sample": false, "description": "1 VIAL in 1 BLISTER PACK (0067-2001-14) / 8 TABLET, FILM COATED in 1 VIAL", "package_ndc": "0067-2001-14", "marketing_start_date": "20210131"}], "brand_name": "Excedrin Extra Strength Pain Reliever", "product_id": "0067-2001_155eb367-99df-1f50-e063-6294a90a21d6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "Decreased Prostaglandin Production [PE]", "Methylxanthine [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]", "Xanthines [CS]"], "product_ndc": "0067-2001", "generic_name": "Acetaminophen, Aspirin (NSAID), and Caffeine", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Excedrin", "brand_name_suffix": "Extra Strength Pain Reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "ASPIRIN", "strength": "250 mg/1"}, {"name": "CAFFEINE", "strength": "65 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190315", "listing_expiration_date": "20261231"}