NDC 72789-012 – Methocarbamol

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

Human Prescription Drug

Product NDC72789-012

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 (5)

Package NDCDescriptionSince
72789-012-1818 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-18)Dec 19, 2019
72789-012-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-20)Sep 20, 2019
72789-012-2424 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-24)May 5, 2021
72789-012-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-30)Aug 10, 2021
72789-012-4040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-40)Jun 16, 2020

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