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Methocarbamol - 49999-048-20 - (Methocarbamol)

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Drug Information of Methocarbamol

Product NDC: 49999-048
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: 49999-048
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085159
Marketing Category: ANDA
Start Marketing Date: 20111116

Package Information of Methocarbamol

Package NDC: 49999-048-20
Package Description: 20 TABLET in 1 BOTTLE (49999-048-20)

NDC Information of Methocarbamol

NDC Code 49999-048-20
Proprietary Name Methocarbamol
Package Description 20 TABLET in 1 BOTTLE (49999-048-20)
Product NDC 49999-048
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methocarbamol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111116
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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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