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NDC 72789-0012-40 Methocarbamol 500 mg/1 Details

Methocarbamol 500 mg/1

Methocarbamol is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is METHOCARBAMOL.

MedlinePlus Drug Summary

Methocarbamol is used with rest, physical therapy, and other measures to relax muscles and relieve pain and discomfort caused by strains, sprains, and other muscle injuries. Methocarbamol is in a class of medications called muscle relaxants. It works by slowing activity in the nervous system to allow the body to relax

Related Packages: 72789-0012-40
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Methocarbamol

Product Information

NDC	72789-0012
Product ID	72789-012_f93b9f48-d0eb-8af4-e053-6394a90afa28
Associated GPIs	75100070000305
GCN Sequence Number	004654
GCN Sequence Number Description	methocarbamol TABLET 500 MG ORAL
HIC3	H6H
HIC3 Description	SKELETAL MUSCLE RELAXANTS
GCN	17892
HICL Sequence Number	001938
HICL Sequence Number Description	METHOCARBAMOL
Brand/Generic	Generic
Proprietary Name	Methocarbamol
Proprietary Name Suffix	n/a
Non-Proprietary Name	Methocarbamol
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	METHOCARBAMOL
Labeler Name	PD-Rx Pharmaceuticals, Inc.
Pharmaceutical Class	Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA208507
Listing Certified Through	2024-12-31

Package

NDC 72789-0012-40 (72789001240)

Pricing Information	N/A
NDC Package Code	72789-012-40
Billing NDC	72789001240
Package	40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-40)
Marketing Start Date	2020-06-16
NDC Exclude Flag	N