butalbital/acetaminophen/caffeine

Generic: butalbital/acetaminophen/caffeine

Labeler: advanced rx pharmacy of tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name butalbital/acetaminophen/caffeine
Generic Name butalbital/acetaminophen/caffeine
Labeler advanced rx pharmacy of tennessee, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

acetaminophen 300 mg/1, butalbital 50 mg/1, caffeine 40 mg/1

Manufacturer
Advanced Rx Pharmacy of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0215
Product ID 80425-0215_2a9aa22e-db3d-217b-e063-6294a90a4c41
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213321
DEA Schedule ciii
Listing Expiration 2026-12-31
Marketing Start 2023-01-03

Pharmacologic Class

Established (EPC)
barbiturate [epc] central nervous system stimulant [epc] methylxanthine [epc]
Chemical Structure
barbiturates [cs] xanthines [cs]
Physiologic Effect
central nervous system stimulation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 804250215
Hyphenated Format 80425-0215

Supplemental Identifiers

RxCUI
889520
UNII
362O9ITL9D KHS0AZ4JVK 3G6A5W338E
NUI
N0000175693 M0002177 N0000175739 N0000175729 N0000175790 M0023046

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/caffeine (source: ndc)
Application Number ANDA213321 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
  • 50 mg/1
  • 40 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (80425-0215-1)
source: ndc

Packages (1)

Ingredients (3)

acetaminophen (300 mg/1) butalbital (50 mg/1) caffeine (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a9aa22e-db3d-217b-e063-6294a90a4c41", "openfda": {"nui": ["N0000175693", "M0002177", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "unii": ["362O9ITL9D", "KHS0AZ4JVK", "3G6A5W338E"], "rxcui": ["889520"], "spl_set_id": ["f16429e2-4944-5bbc-e053-2a95a90ab528"], "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": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (80425-0215-1)", "package_ndc": "80425-0215-1", "marketing_start_date": "20230103"}], "brand_name": "Butalbital/Acetaminophen/Caffeine", "product_id": "80425-0215_2a9aa22e-db3d-217b-e063-6294a90a4c41", "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": "80425-0215", "dea_schedule": "CIII", "generic_name": "Butalbital/Acetaminophen/Caffeine", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Butalbital/Acetaminophen/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": "20230103", "listing_expiration_date": "20261231"}