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CHLORZOXAZONE - 16590-478-71 - (CHLORZOXAZONE)

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Drug Information of CHLORZOXAZONE

Product NDC: 16590-478
Proprietary Name: CHLORZOXAZONE
Non Proprietary Name: CHLORZOXAZONE
Active Ingredient(s): 500    mg/1 & nbsp;   CHLORZOXAZONE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CHLORZOXAZONE

Product NDC: 16590-478
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089859
Marketing Category: ANDA
Start Marketing Date: 20081223

Package Information of CHLORZOXAZONE

Package NDC: 16590-478-71
Package Description: 100 TABLET in 1 BOTTLE (16590-478-71)

NDC Information of CHLORZOXAZONE

NDC Code 16590-478-71
Proprietary Name CHLORZOXAZONE
Package Description 100 TABLET in 1 BOTTLE (16590-478-71)
Product NDC 16590-478
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CHLORZOXAZONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081223
Marketing Category Name ANDA
Labeler Name STAT Rx USA LLC
Substance Name CHLORZOXAZONE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of CHLORZOXAZONE


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