NDC 72162-2488 – Methocarbamol Tablets, USP, 750 mg

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

Human Prescription Drug

Product NDC72162-2488

Product details

Brand name
Methocarbamol Tablets, USP, 750 mg
Generic name
Methocarbamol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212623
Marketed since
January 1, 2024
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol Tablets, USP, 750 mg →

Package NDC codes (2)

Package NDCDescriptionSince
72162-2488-1100 TABLET, FILM COATED in 1 BOTTLE (72162-2488-1)May 5, 2025
72162-2488-5500 TABLET, FILM COATED in 1 BOTTLE (72162-2488-5)May 5, 2025

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