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
- 85766-060_4e912acb-600b-b342-e063-6394a90a4b4f
- Product NDC
- 85766-060
- Form
- TABLET, FILM COATED
- Composition / generic term
- Methocarbamol
- Labeler
- Sportpharm LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200812
- Source listing expiry
- 20271231
Source-listed ingredients
- METHOCARBAMOL — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (85766-060-01) · 85766-060-01
- 500 TABLET, FILM COATED in 1 BOTTLE (85766-060-05) · 85766-060-05
- 21 TABLET, FILM COATED in 1 BOTTLE (85766-060-21) · 85766-060-21
- 28 TABLET, FILM COATED in 1 BOTTLE (85766-060-28) · 85766-060-28
- 30 TABLET, FILM COATED in 1 BOTTLE (85766-060-30) · 85766-060-30
- 42 TABLET, FILM COATED in 1 BOTTLE (85766-060-42) · 85766-060-42
- 60 TABLET, FILM COATED in 1 BOTTLE (85766-060-60) · 85766-060-60
- 90 TABLET, FILM COATED in 1 BOTTLE (85766-060-90) · 85766-060-90
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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