United States · FDA National Drug Code directory

butalbital and acetaminophen

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
75907-008_a511d156-e9d4-8158-9833-b4e6653b4bcf
Product NDC
75907-008
Form
CAPSULE
Composition / generic term
butalbital and acetaminophen
Labeler
Dr. Reddy's Labratories Inc.
Marketing category
ANDA
Marketing start / end (source format)
20240901
Source listing expiry
20261231

Source-listed ingredients

  • BUTALBITAL — 50 mg/1
  • ACETAMINOPHEN — 300 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE in 1 BOTTLE (75907-008-01) · 75907-008-01

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 →
butalbital and acetaminophen — United States | Molindra Medicines