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NDC 70934-0756-30 Methocarbamol 750 mg/1 Details

Methocarbamol 750 mg/1

Methocarbamol is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. dba Northwind Pharmaceuticals. 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: 70934-0756-30
Last Updated: 05/12/2024
MedLinePlus Full Drug Details: Methocarbamol

Product Information

NDC	70934-0756
Product ID	70934-756_de1d004b-f814-03a5-e053-2a95a90a2b58
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Methocarbamol
Proprietary Name Suffix	n/a
Non-Proprietary Name	Methocarbamol Tablets
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, COATED
Route	ORAL
Active Ingredient Strength	750
Active Ingredient Units	mg/1
Substance Name	METHOCARBAMOL
Labeler Name	Denton Pharma, Inc. dba Northwind Pharmaceuticals
Pharmaceutical Class	Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA209312
Listing Certified Through	n/a

Package

NDC 70934-0756-30 (70934075630)

Pricing Information	N/A
NDC Package Code	70934-756-30
Billing NDC	70934075630
Package	30 TABLET, COATED in 1 BOTTLE, PLASTIC (70934-756-30)
Marketing Start Date	2022-05-03
NDC Exclude Flag	N