NDC 67046-0340 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC67046-0340

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol Tablets
Labeler
Coupler LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209312
Marketed since
August 31, 2026
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (1)

Package NDCDescriptionSince
67046-0340-330 TABLET, COATED in 1 BLISTER PACK (67046-0340-3)Aug 31, 2026

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