NDC 76420-040 – Methocarbamol

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

Human Prescription Drug

Product NDC76420-040

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
Asclemed USA, Inc.
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
76420-040-3030 TABLET, FILM COATED in 1 BOTTLE (76420-040-30)Jan 23, 2020
76420-040-6060 TABLET, FILM COATED in 1 BOTTLE (76420-040-60)Jan 23, 2020

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