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Methocarbamol - 0904-2364-60 - (Methocarbamol)

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Drug Information of Methocarbamol

Product NDC: 0904-2364
Proprietary Name: Methocarbamol
Non Proprietary Name: Methocarbamol
Active Ingredient(s): 500    mg/1 & nbsp;   Methocarbamol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methocarbamol

Product NDC: 0904-2364
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085159
Marketing Category: ANDA
Start Marketing Date: 19760811

Package Information of Methocarbamol

Package NDC: 0904-2364-60
Package Description: 100 TABLET in 1 BOTTLE (0904-2364-60)

NDC Information of Methocarbamol

NDC Code 0904-2364-60
Proprietary Name Methocarbamol
Package Description 100 TABLET in 1 BOTTLE (0904-2364-60)
Product NDC 0904-2364
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methocarbamol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19760811
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name METHOCARBAMOL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Methocarbamol


General Information