Lorzone - 68025-046-02 - (chlorzoxazone)

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Drug Information of Lorzone

Product NDC: 68025-046
Proprietary Name: Lorzone
Non Proprietary Name: chlorzoxazone
Active Ingredient(s): 375    mg/1 & nbsp;   chlorzoxazone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lorzone

Product NDC: 68025-046
Labeler Name: Vertical Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040861
Marketing Category: ANDA
Start Marketing Date: 20111001

Package Information of Lorzone

Package NDC: 68025-046-02
Package Description: 2 POUCH in 1 BOX, UNIT-DOSE (68025-046-02) > 1 TABLET in 1 POUCH (68025-046-01)

NDC Information of Lorzone

NDC Code 68025-046-02
Proprietary Name Lorzone
Package Description 2 POUCH in 1 BOX, UNIT-DOSE (68025-046-02) > 1 TABLET in 1 POUCH (68025-046-01)
Product NDC 68025-046
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name chlorzoxazone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111001
Marketing Category Name ANDA
Labeler Name Vertical Pharmaceuticals, Inc.
Substance Name CHLORZOXAZONE
Strength Number 375
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Lorzone


General Information