NDC 80425-0138 – Methocarbamol

Methocarbamol 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC80425-0138

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208507
Marketed since
January 15, 2018
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (2)

Package NDCDescriptionSince
80425-0138-160 TABLET, FILM COATED in 1 BOTTLE (80425-0138-1)Jan 15, 2018
80425-0138-290 TABLET, FILM COATED in 1 BOTTLE (80425-0138-2)Jan 15, 2018

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