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Methocarbamol - 42549-652-12 - (Methocarbamol)

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Drug Information of Methocarbamol

Product NDC: 42549-652
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: 42549-652
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084277
Marketing Category: ANDA
Start Marketing Date: 19871101

Package Information of Methocarbamol

Package NDC: 42549-652-12
Package Description: 120 TABLET in 1 BOTTLE (42549-652-12)

NDC Information of Methocarbamol

NDC Code 42549-652-12
Proprietary Name Methocarbamol
Package Description 120 TABLET in 1 BOTTLE (42549-652-12)
Product NDC 42549-652
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 STAT Rx USA 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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