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Methocarbamol - 55289-164-60 - (Methocarbamol)

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Drug Information of Methocarbamol

Product NDC: 55289-164
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: 55289-164
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084276
Marketing Category: ANDA
Start Marketing Date: 19871101

Package Information of Methocarbamol

Package NDC: 55289-164-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (55289-164-60)

NDC Information of Methocarbamol

NDC Code 55289-164-60
Proprietary Name Methocarbamol
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (55289-164-60)
Product NDC 55289-164
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 PD-Rx 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


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