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
- 69584-612_869612eb-80c5-498d-b4c1-a4f26e93a542
- Product NDC
- 69584-612
- Form
- TABLET
- Composition / generic term
- methocarbamol
- Labeler
- Oxford Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190815
- Source listing expiry
- 20271231
Source-listed ingredients
- METHOCARBAMOL — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE (69584-612-09) · 69584-612-09
- 100 TABLET in 1 BOTTLE (69584-612-10) · 69584-612-10
- 500 TABLET in 1 BOTTLE (69584-612-50) · 69584-612-50
- 1000 TABLET in 1 BOTTLE (69584-612-90) · 69584-612-90
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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