butalbital, aspirin, and caffeine
Generic: butalbital, aspirin, and caffeine
Labeler: westminster pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
butalbital, aspirin, and caffeine
Generic Name
butalbital, aspirin, and caffeine
Labeler
westminster pharmaceuticals, llc
Dosage Form
CAPSULE
Routes
Active Ingredients
aspirin 325 mg/1, butalbital 50 mg/1, caffeine 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69367-416
Product ID
69367-416_ac7dfe8b-b751-4ee0-8f41-5e3f4b934c6f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078149
DEA Schedule
ciii
Listing Expiration
2026-12-31
Marketing Start
2025-10-24
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69367416
Hyphenated Format
69367-416
Supplemental Identifiers
RxCUI
UPC
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
butalbital, aspirin, and caffeine (source: ndc)
Generic Name
butalbital, aspirin, and caffeine (source: ndc)
Application Number
ANDA078149 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 50 mg/1
- 40 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (69367-416-01)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ac7dfe8b-b751-4ee0-8f41-5e3f4b934c6f", "openfda": {"nui": ["N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832", "N0000175693", "M0002177", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "upc": ["0369367416016"], "unii": ["R16CO5Y76E", "KHS0AZ4JVK", "3G6A5W338E"], "rxcui": ["238134"], "spl_set_id": ["ac6ceec2-72d8-4901-9d30-278965a79049"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]", "Barbiturates [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]", "Barbiturate [EPC]", "Central Nervous System Stimulant [EPC]", "Methylxanthine [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (69367-416-01)", "package_ndc": "69367-416-01", "marketing_start_date": "20251024"}], "brand_name": "BUTALBITAL, ASPIRIN, AND CAFFEINE", "product_id": "69367-416_ac7dfe8b-b751-4ee0-8f41-5e3f4b934c6f", "dosage_form": "CAPSULE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Barbiturate [EPC]", "Barbiturates [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": "69367-416", "dea_schedule": "CIII", "generic_name": "BUTALBITAL, ASPIRIN, AND CAFFEINE", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUTALBITAL, ASPIRIN, AND CAFFEINE", "active_ingredients": [{"name": "ASPIRIN", "strength": "325 mg/1"}, {"name": "BUTALBITAL", "strength": "50 mg/1"}, {"name": "CAFFEINE", "strength": "40 mg/1"}], "application_number": "ANDA078149", "marketing_category": "ANDA", "marketing_start_date": "20251024", "listing_expiration_date": "20261231"}