butalbital, acetaminophen and caffeine
Generic: butalbital, acetaminophen, and caffeine
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
butalbital, acetaminophen and caffeine
Generic Name
butalbital, acetaminophen, and caffeine
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 325 mg/1, butalbital 50 mg/1, caffeine 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4467
Product ID
70518-4467_495eb3fc-ff88-fce6-e063-6294a90a8b4c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040511
DEA Schedule
ciii
Listing Expiration
2027-12-31
Marketing Start
2025-09-05
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184467
Hyphenated Format
70518-4467
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 and caffeine (source: ndc)
Generic Name
butalbital, acetaminophen, and caffeine (source: ndc)
Application Number
ANDA040511 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 50 mg/1
- 40 mg/1
Packaging
- 20 TABLET in 1 BOTTLE, PLASTIC (70518-4467-0)
- 60 TABLET in 1 BOTTLE, PLASTIC (70518-4467-1)
- 60 TABLET in 1 BOTTLE, PLASTIC (70518-4467-2)
- 180 TABLET in 1 BOTTLE, PLASTIC (70518-4467-3)
Packages (4)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "495eb3fc-ff88-fce6-e063-6294a90a8b4c", "openfda": {"nui": ["N0000175693", "M0002177", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "unii": ["362O9ITL9D", "KHS0AZ4JVK", "3G6A5W338E"], "rxcui": ["238154"], "spl_set_id": ["157fd0d2-aa54-406c-bcdb-dad531de3ce7"], "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": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (70518-4467-0)", "package_ndc": "70518-4467-0", "marketing_start_date": "20250905"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-4467-1)", "package_ndc": "70518-4467-1", "marketing_start_date": "20251204"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-4467-2)", "package_ndc": "70518-4467-2", "marketing_start_date": "20251210"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-4467-3)", "package_ndc": "70518-4467-3", "marketing_start_date": "20260126"}], "brand_name": "Butalbital, Acetaminophen and Caffeine", "product_id": "70518-4467_495eb3fc-ff88-fce6-e063-6294a90a8b4c", "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": "70518-4467", "dea_schedule": "CIII", "generic_name": "Butalbital, Acetaminophen, and Caffeine", "labeler_name": "REMEDYREPACK INC.", "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": "ANDA040511", "marketing_category": "ANDA", "marketing_start_date": "20250905", "listing_expiration_date": "20271231"}