butalbital, acetaminophen and caffeine

Generic: butalbital, acetaminophen and caffeine

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name butalbital, acetaminophen and caffeine
Generic Name butalbital, acetaminophen and caffeine
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, butalbital 50 mg/1, caffeine 40 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-520
Product ID 63187-520_42b76389-6fa2-49a5-b435-672d3862c6f3
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)
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 63187520
Hyphenated Format 63187-520

Supplemental Identifiers

RxCUI
238154
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 and caffeine (source: ndc)
Generic Name butalbital, acetaminophen and caffeine (source: ndc)
Application Number ANDA089175 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 50 mg/1
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (63187-520-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (63187-520-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (63187-520-90)
source: ndc

Packages (3)

63187-520-30 30 TABLET in 1 BOTTLE, PLASTIC (63187-520-30) 63187-520-60 60 TABLET in 1 BOTTLE, PLASTIC (63187-520-60) 63187-520-90 90 TABLET in 1 BOTTLE, PLASTIC (63187-520-90)

Ingredients (3)

acetaminophen (325 mg/1) butalbital (50 mg/1) caffeine (40 mg/1)

Linked Drug Pages (1)

butalbital, acetaminophen and caffeine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "42b76389-6fa2-49a5-b435-672d3862c6f3", "openfda": {"nui": ["N0000175693", "M0002177", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "unii": ["362O9ITL9D", "KHS0AZ4JVK", "3G6A5W338E"], "rxcui": ["238154"], "spl_set_id": ["1bde13a5-cdd4-4bc2-8aeb-32e4dc157293"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (63187-520-30)", "package_ndc": "63187-520-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (63187-520-60)", "package_ndc": "63187-520-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (63187-520-90)", "package_ndc": "63187-520-90", "marketing_start_date": "20181201"}], "brand_name": "butalbital, acetaminophen and caffeine", "product_id": "63187-520_42b76389-6fa2-49a5-b435-672d3862c6f3", "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": "63187-520", "dea_schedule": "CIII", "generic_name": "butalbital, acetaminophen and caffeine", "labeler_name": "Proficient Rx LP", "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"}