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
- 68071-3859_485d986c-7678-9b95-e063-6394a90a43ea
- Product NDC
- 68071-3859
- Form
- TABLET, FILM COATED
- Composition / generic term
- Methocarbamol
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
- 20 TABLET, FILM COATED in 1 BOTTLE (68071-3859-2) · 68071-3859-2
- 30 TABLET, FILM COATED in 1 BOTTLE (68071-3859-3) · 68071-3859-3
- 90 TABLET, FILM COATED in 1 BOTTLE (68071-3859-9) · 68071-3859-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →