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Carisoprodol - 68788-2582-9 - (Carisoprodol)

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Drug Information of Carisoprodol

Product NDC: 68788-2582
Proprietary Name: Carisoprodol
Non Proprietary Name: Carisoprodol
Active Ingredient(s): 350    mg/1 & nbsp;   Carisoprodol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Carisoprodol

Product NDC: 68788-2582
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040245
Marketing Category: ANDA
Start Marketing Date: 19970908

Package Information of Carisoprodol

Package NDC: 68788-2582-9
Package Description: 90 TABLET in 1 BOTTLE (68788-2582-9)

NDC Information of Carisoprodol

NDC Code 68788-2582-9
Proprietary Name Carisoprodol
Package Description 90 TABLET in 1 BOTTLE (68788-2582-9)
Product NDC 68788-2582
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carisoprodol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970908
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
Substance Name CARISOPRODOL
Strength Number 350
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Carisoprodol


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