← FDA DRUG APPROVALS
FDA ANDA · ANDA204733
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Sponsor: AUROLIFE PHARMA LLC
APPLICATION
ANDA204733
TYPE
ANDA
ORIGINAL APPROVAL
2018-09-26
LATEST ACTION
2025-08-04
ROUTE
ORAL
DOSAGE FORM
CAPSULE
MARKETING STATUS
Prescription
Products
BUTALBITAL, ACETAMINOPHEN AND CAFFEINEPrescription
ACETAMINOPHEN 325MG, BUTALBITAL 50MG, CAFFEINE 40MG · CAPSULE · ORAL
Approval history
2025-08-04Labeling · Supplement 1 · standardAP
2018-09-26UNKNOWN · OriginalAP
Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.
Weekly Briefing
Read a past issue →Get the Weekly GxP Briefing
Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.