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
- 71335-2795_2dfcd0f2-2660-425b-81d9-0035e379e61b
- Product NDC
- 71335-2795
- Form
- TABLET, FILM COATED
- Composition / generic term
- Methocarbamol
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200812
- Source listing expiry
- 20261231
Source-listed ingredients
- METHOCARBAMOL — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET, FILM COATED in 1 BOTTLE (71335-2795-0) · 71335-2795-0
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-2795-1) · 71335-2795-1
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-2795-2) · 71335-2795-2
- 40 TABLET, FILM COATED in 1 BOTTLE (71335-2795-3) · 71335-2795-3
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-2795-4) · 71335-2795-4
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-2795-5) · 71335-2795-5
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-2795-6) · 71335-2795-6
- 112 TABLET, FILM COATED in 1 BOTTLE (71335-2795-7) · 71335-2795-7
- 21 TABLET, FILM COATED in 1 BOTTLE (71335-2795-8) · 71335-2795-8
- 84 TABLET, FILM COATED in 1 BOTTLE (71335-2795-9) · 71335-2795-9
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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