acetaminophen aspirin and caffeine
Generic: acetaminophen, aspirin and caffeine
Labeler: better living brands, llcDrug Facts
Product Profile
Brand Name
acetaminophen aspirin and caffeine
Generic Name
acetaminophen, aspirin and caffeine
Labeler
better living brands, llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
acetaminophen 250 mg/1, aspirin 250 mg/1, caffeine 65 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
21130-074
Product ID
21130-074_068e2ba0-2db2-4c12-ad9e-47a7130c2a22
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA211695
Listing Expiration
2026-12-31
Marketing Start
2023-08-11
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
21130074
Hyphenated Format
21130-074
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
acetaminophen aspirin and caffeine (source: ndc)
Generic Name
acetaminophen, aspirin and caffeine (source: ndc)
Application Number
ANDA211695 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
- 65 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (21130-074-07) / 24 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (21130-074-14) / 50 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (21130-074-21) / 100 TABLET, FILM COATED in 1 BOTTLE
Packages (3)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "068e2ba0-2db2-4c12-ad9e-47a7130c2a22", "openfda": {"nui": ["N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "unii": ["362O9ITL9D", "R16CO5Y76E", "3G6A5W338E"], "rxcui": ["308297"], "spl_set_id": ["f8050cae-8619-f49b-e053-6294a90ad9e6"], "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": ["Better Living Brands, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-074-07) / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "21130-074-07", "marketing_start_date": "20230811"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-074-14) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "21130-074-14", "marketing_start_date": "20230811"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-074-21) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "21130-074-21", "marketing_start_date": "20230811"}], "brand_name": "ACETAMINOPHEN ASPIRIN AND CAFFEINE", "product_id": "21130-074_068e2ba0-2db2-4c12-ad9e-47a7130c2a22", "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": "21130-074", "generic_name": "acetaminophen, aspirin and caffeine", "labeler_name": "Better Living Brands, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN ASPIRIN AND CAFFEINE", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "ASPIRIN", "strength": "250 mg/1"}, {"name": "CAFFEINE", "strength": "65 mg/1"}], "application_number": "ANDA211695", "marketing_category": "ANDA", "marketing_start_date": "20230811", "listing_expiration_date": "20261231"}