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
- 50090-3556_3ec36912-826c-4923-9fea-047e31264e0c
- Product NDC
- 50090-3556
- Form
- TABLET, COATED
- Composition / generic term
- Methocarbamol Tablets
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180702
- Source listing expiry
- 20261231
Source-listed ingredients
- METHOCARBAMOL — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-0) · 50090-3556-0
- 40 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-1) · 50090-3556-1
- 28 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-2) · 50090-3556-2
- 30 TABLET, COATED in 1 BOTTLE (50090-3556-3) · 50090-3556-3
- 60 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-4) · 50090-3556-4
- 100 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-6) · 50090-3556-6
- 12 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-7) · 50090-3556-7
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 →