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Methocarbamol - 68788-9076-1 - (methocarbamol)

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Drug Information of Methocarbamol

Product NDC: 68788-9076
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: 68788-9076
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040489
Marketing Category: ANDA
Start Marketing Date: 20030129

Package Information of Methocarbamol

Package NDC: 68788-9076-1
Package Description: 100 TABLET in 1 BOTTLE, DISPENSING (68788-9076-1)

NDC Information of Methocarbamol

NDC Code 68788-9076-1
Proprietary Name Methocarbamol
Package Description 100 TABLET in 1 BOTTLE, DISPENSING (68788-9076-1)
Product NDC 68788-9076
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methocarbamol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030129
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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