butalbital, acetaminophen, caffeine
Generic: butalbital, acetaminophen, and caffeine
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
butalbital, acetaminophen, caffeine
Generic Name
butalbital, acetaminophen, and caffeine
Labeler
proficient rx lp
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 325 mg/1, butalbital 50 mg/1, caffeine 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-510
Product ID
71205-510_8e082b99-7601-499d-b32d-d84e4174d425
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209587
DEA Schedule
ciii
Listing Expiration
2026-12-31
Marketing Start
2019-03-05
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205510
Hyphenated Format
71205-510
Supplemental Identifiers
RxCUI
UNII
NUI
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, caffeine (source: ndc)
Generic Name
butalbital, acetaminophen, and caffeine (source: ndc)
Application Number
ANDA209587 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 50 mg/1
- 40 mg/1
Packaging
- 14 TABLET in 1 BOTTLE (71205-510-14)
- 30 TABLET in 1 BOTTLE (71205-510-30)
- 60 TABLET in 1 BOTTLE (71205-510-60)
- 90 TABLET in 1 BOTTLE (71205-510-90)
Packages (4)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8e082b99-7601-499d-b32d-d84e4174d425", "openfda": {"nui": ["N0000175693", "M0002177", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "unii": ["362O9ITL9D", "KHS0AZ4JVK", "3G6A5W338E"], "rxcui": ["238154"], "spl_set_id": ["3cf799b4-c785-4ae2-908b-c42e426733dc"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE (71205-510-14)", "package_ndc": "71205-510-14", "marketing_start_date": "20201125"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-510-30)", "package_ndc": "71205-510-30", "marketing_start_date": "20201125"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-510-60)", "package_ndc": "71205-510-60", "marketing_start_date": "20201125"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-510-90)", "package_ndc": "71205-510-90", "marketing_start_date": "20201125"}], "brand_name": "Butalbital, Acetaminophen, Caffeine", "product_id": "71205-510_8e082b99-7601-499d-b32d-d84e4174d425", "dosage_form": "TABLET", "pharm_class": ["Barbiturate [EPC]", "Barbiturates [CS]", "Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "71205-510", "dea_schedule": "CIII", "generic_name": "Butalbital, Acetaminophen, and Caffeine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Butalbital, Acetaminophen, Caffeine", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "BUTALBITAL", "strength": "50 mg/1"}, {"name": "CAFFEINE", "strength": "40 mg/1"}], "application_number": "ANDA209587", "marketing_category": "ANDA", "marketing_start_date": "20190305", "listing_expiration_date": "20261231"}