butalbital, acetaminophen and caffeine
Generic: butalbital, acetaminophen and caffeine
Labeler: granules pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
butalbital, acetaminophen and caffeine
Generic Name
butalbital, acetaminophen and caffeine
Labeler
granules pharmaceuticals inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
acetaminophen 300 mg/1, butalbital 50 mg/1, caffeine 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70010-044
Product ID
70010-044_0bbc89b6-8700-134d-e063-6394a90a94f8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213321
Listing Expiration
2026-12-31
Marketing Start
2020-05-05
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70010044
Hyphenated Format
70010-044
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
ANDA213321 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 300 mg/1
- 50 mg/1
- 40 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (70010-044-01)
- 500 CAPSULE in 1 BOTTLE (70010-044-05)
Packages (2)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0bbc89b6-8700-134d-e063-6394a90a94f8", "openfda": {"nui": ["N0000175693", "M0002177", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "upc": ["0370010044012"], "unii": ["362O9ITL9D", "KHS0AZ4JVK", "3G6A5W338E"], "rxcui": ["889520"], "spl_set_id": ["2407efce-b77e-4072-bc4b-62c789d01e1a"], "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": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (70010-044-01)", "package_ndc": "70010-044-01", "marketing_start_date": "20200505"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (70010-044-05)", "package_ndc": "70010-044-05", "marketing_start_date": "20200505"}], "brand_name": "Butalbital, Acetaminophen and Caffeine", "product_id": "70010-044_0bbc89b6-8700-134d-e063-6394a90a94f8", "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": "70010-044", "generic_name": "Butalbital, Acetaminophen and Caffeine", "labeler_name": "Granules Pharmaceuticals Inc.", "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": "ANDA213321", "marketing_category": "ANDA", "marketing_start_date": "20200505", "listing_expiration_date": "20261231"}