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Methocarbamol - 21695-078-30 - (Methocarbamol)

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Drug Information of Methocarbamol

Product NDC: 21695-078
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: 21695-078
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085159
Marketing Category: ANDA
Start Marketing Date: 20000101

Package Information of Methocarbamol

Package NDC: 21695-078-30
Package Description: 30 TABLET in 1 BOTTLE (21695-078-30)

NDC Information of Methocarbamol

NDC Code 21695-078-30
Proprietary Name Methocarbamol
Package Description 30 TABLET in 1 BOTTLE (21695-078-30)
Product NDC 21695-078
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methocarbamol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000101
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
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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