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Chlorzoxazone - 21695-569-90 - (Chlorzoxazone)

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Drug Information of Chlorzoxazone

Product NDC: 21695-569
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: 21695-569
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089895
Marketing Category: ANDA
Start Marketing Date: 19880504

Package Information of Chlorzoxazone

Package NDC: 21695-569-90
Package Description: 90 TABLET in 1 BOTTLE (21695-569-90)

NDC Information of Chlorzoxazone

NDC Code 21695-569-90
Proprietary Name Chlorzoxazone
Package Description 90 TABLET in 1 BOTTLE (21695-569-90)
Product NDC 21695-569
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlorzoxazone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880504
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name CHLORZOXAZONE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Chlorzoxazone


General Information