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Methocarbamol - 52959-099-20 - (Methocarbamol)

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Drug Information of Methocarbamol

Product NDC: 52959-099
Proprietary Name: Methocarbamol
Non Proprietary Name: Methocarbamol
Active Ingredient(s): 750    mg/1 & nbsp;   Methocarbamol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methocarbamol

Product NDC: 52959-099
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084276
Marketing Category: ANDA
Start Marketing Date: 19871101

Package Information of Methocarbamol

Package NDC: 52959-099-20
Package Description: 20 TABLET in 1 BOTTLE (52959-099-20)

NDC Information of Methocarbamol

NDC Code 52959-099-20
Proprietary Name Methocarbamol
Package Description 20 TABLET in 1 BOTTLE (52959-099-20)
Product NDC 52959-099
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methocarbamol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19871101
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name METHOCARBAMOL
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Methocarbamol


General Information