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
- 70010-770_56016dcc-153e-f9be-e063-6294a90ab407
- Product NDC
- 70010-770
- Form
- TABLET, COATED
- Composition / generic term
- Methocarbamol Tablets
- Labeler
- Granules Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180702
- Source listing expiry
- 20271231
Source-listed ingredients
- METHOCARBAMOL — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, COATED in 1 BOTTLE (70010-770-01) · 70010-770-01
- 500 TABLET, COATED in 1 BOTTLE (70010-770-05) · 70010-770-05
- 1000 TABLET, COATED in 1 BOTTLE (70010-770-10) · 70010-770-10
- 24 TABLET, COATED in 1 BOTTLE (70010-770-35) · 70010-770-35
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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