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
- 62207-770_44e3ccde-759c-0def-e063-6394a90ab87d
- Product NDC
- 62207-770
- Form
- TABLET, COATED
- Composition / generic term
- Methocarbamol Tablets
- Labeler
- Granules India Ltd
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180515
- Source listing expiry
- 20261231
Source-listed ingredients
- METHOCARBAMOL — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 24 TABLET, COATED in 1 BOTTLE (62207-770-41) · 62207-770-41
- 100 TABLET, COATED in 1 BOTTLE (62207-770-43) · 62207-770-43
- 500 TABLET, COATED in 1 BOTTLE (62207-770-47) · 62207-770-47
- 1000 TABLET, COATED in 1 BOTTLE (62207-770-49) · 62207-770-49
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 →