butalbital, acetaminophen and caffeine
Generic: butalbital, acetaminophen and caffeine
Labeler: chartwell rx, llcDrug Facts
Product Profile
Brand Name
butalbital, acetaminophen and caffeine
Generic Name
butalbital, acetaminophen and caffeine
Labeler
chartwell rx, llc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 325 mg/1, butalbital 50 mg/1, caffeine 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62135-751
Product ID
62135-751_458c0456-32bb-ff23-e063-6394a90aceea
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA089175
DEA Schedule
ciii
Listing Expiration
2026-12-31
Marketing Start
1987-01-21
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62135751
Hyphenated Format
62135-751
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
ANDA089175 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 50 mg/1
- 40 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (62135-751-01)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "458c0456-32bb-ff23-e063-6394a90aceea", "openfda": {"nui": ["N0000175693", "M0002177", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "upc": ["0362135751012"], "unii": ["362O9ITL9D", "KHS0AZ4JVK", "3G6A5W338E"], "rxcui": ["238154"], "spl_set_id": ["77776146-c6e6-478c-b30e-2b729e758400"], "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": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62135-751-01)", "package_ndc": "62135-751-01", "marketing_start_date": "20230825"}], "brand_name": "BUTALBITAL, ACETAMINOPHEN AND CAFFEINE", "product_id": "62135-751_458c0456-32bb-ff23-e063-6394a90aceea", "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": "62135-751", "dea_schedule": "CIII", "generic_name": "BUTALBITAL, ACETAMINOPHEN AND CAFFEINE", "labeler_name": "Chartwell RX, LLC", "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": "ANDA089175", "marketing_category": "ANDA", "marketing_start_date": "19870121", "listing_expiration_date": "20261231"}