United States · FDA National Drug Code directory

butalbital, acetaminophen and caffeine

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
46672-053_0e845d26-e49d-1fad-e063-6294a90ad864
Product NDC
46672-053
Form
TABLET
Composition / generic term
butalbital, acetaminophen and caffeine
Labeler
Mikart, LLC
Marketing category
ANDA
Marketing start / end (source format)
19870121
Source listing expiry
20261231

Source-listed ingredients

  • BUTALBITAL — 50 mg/1
  • ACETAMINOPHEN — 325 mg/1
  • CAFFEINE — 40 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE, PLASTIC (46672-053-10) · 46672-053-10
  • 500 TABLET in 1 BOTTLE, PLASTIC (46672-053-50) · 46672-053-50

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →