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
- 63323-778_ee1af98a-62a0-4831-b3c1-45607737b32f
- Product NDC
- 63323-778
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Methocarbamol
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180417
- Source listing expiry
- 20261231
Source-listed ingredients
- METHOCARBAMOL — 100 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 CARTON (63323-778-10) / 10 mL in 1 VIAL (63323-778-21) · 63323-778-10
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 →