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
- 82804-954_e4ebe9cf-a274-47c7-b740-4b3d6e9dc52b
- Product NDC
- 82804-954
- Form
- TABLET
- Composition / generic term
- methocarbamol
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190815
- Source listing expiry
- 20271231
Source-listed ingredients
- METHOCARBAMOL — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (82804-954-00) · 82804-954-00
- 30 TABLET in 1 BOTTLE (82804-954-30) · 82804-954-30
- 500 TABLET in 1 BOTTLE (82804-954-55) · 82804-954-55
- 60 TABLET in 1 BOTTLE (82804-954-60) · 82804-954-60
- 120 TABLET in 1 BOTTLE (82804-954-72) · 82804-954-72
- 90 TABLET in 1 BOTTLE (82804-954-90) · 82804-954-90
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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