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
- 71205-167_3f2b80a9-5d79-4c3f-86f6-85621b565835
- Product NDC
- 71205-167
- Form
- TABLET, COATED
- Composition / generic term
- Methocarbamol Tablets
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180702
- Source listing expiry
- 20271231
Source-listed ingredients
- METHOCARBAMOL — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET, COATED in 1 BOTTLE (71205-167-06) · 71205-167-06
- 9 TABLET, COATED in 1 BOTTLE (71205-167-09) · 71205-167-09
- 30 TABLET, COATED in 1 BOTTLE (71205-167-30) · 71205-167-30
- 60 TABLET, COATED in 1 BOTTLE (71205-167-60) · 71205-167-60
- 90 TABLET, COATED in 1 BOTTLE (71205-167-90) · 71205-167-90
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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