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
- 67296-2193_4ff1938d-1f5f-0811-e063-6394a90a9049
- Product NDC
- 67296-2193
- Form
- TABLET, FILM COATED
- Composition / generic term
- Methocarbamol
- Labeler
- Redpharm Drug
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230209
- Source listing expiry
- 20271231
Source-listed ingredients
- METHOCARBAMOL — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET, FILM COATED in 1 BOTTLE (67296-2193-1) · 67296-2193-1
- 24 TABLET, FILM COATED in 1 BOTTLE (67296-2193-2) · 67296-2193-2
- 40 TABLET, FILM COATED in 1 BOTTLE (67296-2193-4) · 67296-2193-4
Source and coverage
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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.
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