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Methocarbamol - 21695-079-07 - (Methocarbamol)

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Drug Information of Methocarbamol

Product NDC: 21695-079
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: 21695-079
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085123
Marketing Category: ANDA
Start Marketing Date: 19760818

Package Information of Methocarbamol

Package NDC: 21695-079-07
Package Description: 7 TABLET in 1 BOTTLE (21695-079-07)

NDC Information of Methocarbamol

NDC Code 21695-079-07
Proprietary Name Methocarbamol
Package Description 7 TABLET in 1 BOTTLE (21695-079-07)
Product NDC 21695-079
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methocarbamol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19760818
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
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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