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Last Updated: December 16, 2025

Details for New Drug Application (NDA): 040489

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NDA 040489 describes METHOCARBAMOL, which is a drug marketed by Dr Reddys, Marsam Pharms Llc, Am Regent, Baxter Hlthcare Corp, Eugia Pharma, Fresenius Kabi Usa, Gland, Monterey Pharms Llc, Navinta Llc, Pharmobedient, Sagent Pharms Inc, Slate Run Pharma, Somerset Theraps Llc, Able, Aiping Pharm Inc, Am Therap, Ani Pharms, Ascot, Aurobindo Pharma Ltd, Bostal, Chartwell Molecular, Clonmel Hlthcare, Granules, Heather, Hetero Labs Ltd Iii, Hikma Intl Pharms, Impax Labs, Inwood Labs, Ivax Sub Teva Pharms, Kv Pharm, Mikart, Mylan, Nylos, Oxford Pharms, Pioneer Pharms, Pointview Hldings, Prinston Inc, Puracap Pharm, Purepac Pharm, Regcon Holdings, Roxane, Sandoz, Solvay, Sun Pharm Industries, Superpharm, Tablicaps, Upsher Smith, Watson Labs, Mcneil, Par Pharm, and Stevens J, and is included in seventy-four NDAs. It is available from sixty-three suppliers. Additional details are available on the METHOCARBAMOL profile page.

The generic ingredient in METHOCARBAMOL is aspirin; methocarbamol. There are twenty-two drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the aspirin; methocarbamol profile page.

Summary for 040489

Tradename:	METHOCARBAMOL
Applicant:	Oxford Pharms
Ingredient:	methocarbamol
Patents:	0

Pharmacology for NDA: 040489

Physiological Effect	Centrally-mediated Muscle Relaxation

Medical Subject Heading (MeSH) Categories for 040489

Muscle Relaxants, Central

Suppliers and Packaging for NDA: 040489

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
METHOCARBAMOL	methocarbamol	TABLET;ORAL	040489	ANDA	GENTEX PHARMA, LLC	15014-910	15014-910-10	100 TABLET in 1 BOTTLE (15014-910-10)
METHOCARBAMOL	methocarbamol	TABLET;ORAL	040489	ANDA	Medsource Pharmaceuticals	45865-242	45865-242-30	30 TABLET in 1 BOTTLE (45865-242-30)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	500MG
Approval Date:	Jan 29, 2003	TE:	AA	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	750MG
Approval Date:	Jan 29, 2003	TE:	AA	RLD:	No

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