ROBAXIN - 16590-981-90 - (METHOCARBAMOL)

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Drug Information of ROBAXIN

Product NDC: 16590-981
Proprietary Name: ROBAXIN
Non Proprietary Name: METHOCARBAMOL
Active Ingredient(s): 750    mg/1 & nbsp;   METHOCARBAMOL
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ROBAXIN

Product NDC: 16590-981
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011011
Marketing Category: NDA
Start Marketing Date: 20030120

Package Information of ROBAXIN

Package NDC: 16590-981-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (16590-981-90)

NDC Information of ROBAXIN

NDC Code 16590-981-90
Proprietary Name ROBAXIN
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (16590-981-90)
Product NDC 16590-981
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METHOCARBAMOL
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030120
Marketing Category Name NDA
Labeler Name STAT RX USA LLC
Substance Name METHOCARBAMOL
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of ROBAXIN


General Information