NDC 72789-110 – Methocarbamol

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

Human Prescription Drug

Product NDC72789-110

Product details

Brand name
Methocarbamol
Generic name
Methocarbamol
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208507
Marketed since
January 15, 2018
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Methocarbamol →

Package NDC codes (1)

Package NDCDescriptionSince
72789-110-4040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-110-40)Sep 8, 2020

Other Methocarbamol products