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
66267-146_1f93738d-24ff-96ac-e063-6294a90a9f84
Product NDC
66267-146
Form
TABLET
Composition / generic term
Methocarbamol
Labeler
NuCare Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20130320
Source listing expiry
20261231

Source-listed ingredients

  • METHOCARBAMOL — 750 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 12 TABLET in 1 BOTTLE (66267-146-12) · 66267-146-12
  • 20 TABLET in 1 BOTTLE (66267-146-20) · 66267-146-20
  • 30 TABLET in 1 BOTTLE (66267-146-30) · 66267-146-30
  • 40 TABLET in 1 BOTTLE (66267-146-40) · 66267-146-40
  • 60 TABLET in 1 BOTTLE (66267-146-60) · 66267-146-60
  • 90 TABLET in 1 BOTTLE (66267-146-90) · 66267-146-90

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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