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Methocarbamol - 31722-534-60 - (Methocarbamol)

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Drug Information of Methocarbamol

Product NDC: 31722-534
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: 31722-534
Labeler Name: Camber Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090200
Marketing Category: ANDA
Start Marketing Date: 20130320

Package Information of Methocarbamol

Package NDC: 31722-534-60
Package Description: 12 BOTTLE in 1 CASE (31722-534-60) > 60 TABLET in 1 BOTTLE

NDC Information of Methocarbamol

NDC Code 31722-534-60
Proprietary Name Methocarbamol
Package Description 12 BOTTLE in 1 CASE (31722-534-60) > 60 TABLET in 1 BOTTLE
Product NDC 31722-534
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methocarbamol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130320
Marketing Category Name ANDA
Labeler Name Camber 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