NDC 71335-2794 – Methocarbamol

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

Human Prescription Drug

Product NDC71335-2794

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213967
Marketed since
February 9, 2023
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2794-015 TABLET, FILM COATED in 1 BOTTLE (71335-2794-0)Oct 13, 2025
71335-2794-114 TABLET, FILM COATED in 1 BOTTLE (71335-2794-1)Oct 13, 2025
71335-2794-230 TABLET, FILM COATED in 1 BOTTLE (71335-2794-2)Oct 13, 2025
71335-2794-320 TABLET, FILM COATED in 1 BOTTLE (71335-2794-3)Oct 13, 2025
71335-2794-460 TABLET, FILM COATED in 1 BOTTLE (71335-2794-4)Oct 13, 2025
71335-2794-5100 TABLET, FILM COATED in 1 BOTTLE (71335-2794-5)Oct 13, 2025
71335-2794-640 TABLET, FILM COATED in 1 BOTTLE (71335-2794-6)Oct 13, 2025
71335-2794-790 TABLET, FILM COATED in 1 BOTTLE (71335-2794-7)Oct 13, 2025
71335-2794-8120 TABLET, FILM COATED in 1 BOTTLE (71335-2794-8)Oct 13, 2025
71335-2794-97 TABLET, FILM COATED in 1 BOTTLE (71335-2794-9)Oct 13, 2025

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