United States · FDA National Drug Code directory

Methocarbamol

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
67296-2197_4c446b06-eba3-8fe1-e063-6294a90aa8b4
Product NDC
67296-2197
Form
TABLET, COATED
Composition / generic term
Methocarbamol Tablets
Labeler
Redpharm Drug
Marketing category
ANDA
Marketing start / end (source format)
20180702
Source listing expiry
20271231

Source-listed ingredients

  • METHOCARBAMOL — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 15 TABLET, COATED in 1 BOTTLE (67296-2197-1) · 67296-2197-1
  • 40 TABLET, COATED in 1 BOTTLE (67296-2197-2) · 67296-2197-2
  • 30 TABLET, COATED in 1 BOTTLE (67296-2197-3) · 67296-2197-3

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 →