butalbital, acetaminophen and caffeine
Generic: butalbital, acetaminophen and caffeine
Labeler: mayne pharmaDrug Facts
Product Profile
Brand Name
butalbital, acetaminophen and caffeine
Generic Name
butalbital, acetaminophen and caffeine
Labeler
mayne pharma
Dosage Form
CAPSULE
Routes
Active Ingredients
acetaminophen 325 mg/1, butalbital 50 mg/1, caffeine 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51862-179
Product ID
51862-179_2b358863-b03e-1f14-e063-6394a90a0fca
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA089007
Marketing Start
2012-04-16
Marketing End
2026-09-19
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51862179
Hyphenated Format
51862-179
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, acetaminophen and caffeine (source: ndc)
Generic Name
butalbital, acetaminophen and caffeine (source: ndc)
Application Number
ANDA089007 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 50 mg/1
- 40 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE, PLASTIC (51862-179-01)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b358863-b03e-1f14-e063-6394a90a0fca", "openfda": {"nui": ["N0000175693", "M0002177", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "upc": ["0351862179015"], "unii": ["362O9ITL9D", "KHS0AZ4JVK", "3G6A5W338E"], "rxcui": ["238153"], "spl_set_id": ["fa88f437-830b-48bc-a44c-fd142963a150"], "pharm_class_cs": ["Barbiturates [CS]", "Xanthines [CS]"], "pharm_class_pe": ["Central Nervous System Stimulation [PE]"], "pharm_class_epc": ["Barbiturate [EPC]", "Central Nervous System Stimulant [EPC]", "Methylxanthine [EPC]"], "manufacturer_name": ["Mayne Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (51862-179-01)", "package_ndc": "51862-179-01", "marketing_end_date": "20260919", "marketing_start_date": "20120416"}], "brand_name": "butalbital, acetaminophen and caffeine", "product_id": "51862-179_2b358863-b03e-1f14-e063-6394a90a0fca", "dosage_form": "CAPSULE", "pharm_class": ["Barbiturate [EPC]", "Barbiturates [CS]", "Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "51862-179", "generic_name": "butalbital, acetaminophen and caffeine", "labeler_name": "Mayne Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "butalbital, acetaminophen and caffeine", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "BUTALBITAL", "strength": "50 mg/1"}, {"name": "CAFFEINE", "strength": "40 mg/1"}], "application_number": "ANDA089007", "marketing_category": "ANDA", "marketing_end_date": "20260919", "marketing_start_date": "20120416"}