butalbital, acetaminophen, and caffeine
Generic: butalbital, acetaminophen, and caffeine
Labeler: northstar rx llcDrug Facts
Product Profile
Brand Name
butalbital, acetaminophen, and caffeine
Generic Name
butalbital, acetaminophen, and caffeine
Labeler
northstar rx llc
Dosage Form
CAPSULE
Routes
Active Ingredients
acetaminophen 300 mg/1, butalbital 50 mg/1, caffeine 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
16714-170
Product ID
16714-170_c884344b-2520-4874-866c-bf9798b506d3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213046
DEA Schedule
ciii
Listing Expiration
2026-12-31
Marketing Start
2020-07-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16714170
Hyphenated Format
16714-170
Supplemental Identifiers
RxCUI
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
ANDA213046 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 300 mg/1
- 50 mg/1
- 40 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (16714-170-01)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c884344b-2520-4874-866c-bf9798b506d3", "openfda": {"nui": ["N0000175693", "M0002177", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "unii": ["362O9ITL9D", "KHS0AZ4JVK", "3G6A5W338E"], "rxcui": ["889520"], "spl_set_id": ["83a63e9b-0a97-4725-bcbb-906fb678ba42"], "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": ["NORTHSTAR RX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (16714-170-01)", "package_ndc": "16714-170-01", "marketing_start_date": "20200923"}], "brand_name": "Butalbital, Acetaminophen, and Caffeine", "product_id": "16714-170_c884344b-2520-4874-866c-bf9798b506d3", "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": "16714-170", "dea_schedule": "CIII", "generic_name": "Butalbital, Acetaminophen, and Caffeine", "labeler_name": "NORTHSTAR RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Butalbital, Acetaminophen, and Caffeine", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "BUTALBITAL", "strength": "50 mg/1"}, {"name": "CAFFEINE", "strength": "40 mg/1"}], "application_number": "ANDA213046", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}