NDC 71335-2795 – Methocarbamol

Methocarbamol 750 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2795

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
August 12, 2020
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
71335-2795-014 TABLET, FILM COATED in 1 BOTTLE (71335-2795-0)Oct 13, 2025
71335-2795-120 TABLET, FILM COATED in 1 BOTTLE (71335-2795-1)Oct 13, 2025
71335-2795-230 TABLET, FILM COATED in 1 BOTTLE (71335-2795-2)Oct 13, 2025
71335-2795-340 TABLET, FILM COATED in 1 BOTTLE (71335-2795-3)Oct 13, 2025
71335-2795-4120 TABLET, FILM COATED in 1 BOTTLE (71335-2795-4)Oct 13, 2025
71335-2795-560 TABLET, FILM COATED in 1 BOTTLE (71335-2795-5)Oct 13, 2025
71335-2795-690 TABLET, FILM COATED in 1 BOTTLE (71335-2795-6)Oct 13, 2025
71335-2795-7112 TABLET, FILM COATED in 1 BOTTLE (71335-2795-7)Oct 13, 2025
71335-2795-821 TABLET, FILM COATED in 1 BOTTLE (71335-2795-8)Oct 13, 2025
71335-2795-984 TABLET, FILM COATED in 1 BOTTLE (71335-2795-9)Oct 13, 2025

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