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Carisoprodol - 55289-049-60 - (Carisoprodol)

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Drug Information of Carisoprodol

Product NDC: 55289-049
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: 55289-049
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087499
Marketing Category: ANDA
Start Marketing Date: 19871101

Package Information of Carisoprodol

Package NDC: 55289-049-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (55289-049-60)

NDC Information of Carisoprodol

NDC Code 55289-049-60
Proprietary Name Carisoprodol
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (55289-049-60)
Product NDC 55289-049
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carisoprodol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19871101
Marketing Category Name ANDA
Labeler Name PD-Rx 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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