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Methocarbamol - 65977-5033-4 - (Methocarbamol)

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Drug Information of Methocarbamol

Product NDC: 65977-5033
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: 65977-5033
Labeler Name: Hetero Drugs Limited Unit III
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090200
Marketing Category: ANDA
Start Marketing Date: 20091106

Package Information of Methocarbamol

Package NDC: 65977-5033-4
Package Description: 1000 TABLET in 1 BOTTLE (65977-5033-4)

NDC Information of Methocarbamol

NDC Code 65977-5033-4
Proprietary Name Methocarbamol
Package Description 1000 TABLET in 1 BOTTLE (65977-5033-4)
Product NDC 65977-5033
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methocarbamol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091106
Marketing Category Name ANDA
Labeler Name Hetero Drugs Limited Unit III
Substance Name METHOCARBAMOL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Methocarbamol


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