acetaminophen, aspirin and caffeine
Generic: acetaminophen, aspirin and caffeine
Labeler: safrel pharmaceuticals, llc.Drug Facts
Product Profile
Brand Name
acetaminophen, aspirin and caffeine
Generic Name
acetaminophen, aspirin and caffeine
Labeler
safrel pharmaceuticals, llc.
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 250 mg/1, aspirin 250 mg/1, caffeine 65 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71309-079
Product ID
71309-079_0ac07846-5f05-dc4b-e063-6394a90ac8ca
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA214039
Listing Expiration
2026-12-31
Marketing Start
2021-04-15
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71309079
Hyphenated Format
71309-079
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
ANDA214039 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
- 65 mg/1
Packaging
- 300 TABLET in 1 BOTTLE (71309-079-03)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0ac07846-5f05-dc4b-e063-6394a90ac8ca", "openfda": {"nui": ["N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "unii": ["362O9ITL9D", "R16CO5Y76E", "3G6A5W338E"], "rxcui": ["308297"], "spl_set_id": ["0ac07846-5f04-dc4b-e063-6394a90ac8ca"], "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": ["Safrel Pharmaceuticals, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (71309-079-03)", "package_ndc": "71309-079-03", "marketing_start_date": "20210415"}], "brand_name": "Acetaminophen, Aspirin and Caffeine", "product_id": "71309-079_0ac07846-5f05-dc4b-e063-6394a90ac8ca", "dosage_form": "TABLET", "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": "71309-079", "generic_name": "Acetaminophen, Aspirin and Caffeine", "labeler_name": "Safrel Pharmaceuticals, 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": "ANDA214039", "marketing_category": "ANDA", "marketing_start_date": "20210415", "listing_expiration_date": "20261231"}