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Carisoprodol and Aspirin - 0185-0724-10 - (Carisoprodol and Aspirin)

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Drug Information of Carisoprodol and Aspirin

Product NDC: 0185-0724
Proprietary Name: Carisoprodol and Aspirin
Non Proprietary Name: Carisoprodol and Aspirin
Active Ingredient(s): 325; 200    mg/1; mg/1 & nbsp;   Carisoprodol and Aspirin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Carisoprodol and Aspirin

Product NDC: 0185-0724
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040116
Marketing Category: ANDA
Start Marketing Date: 19960425

Package Information of Carisoprodol and Aspirin

Package NDC: 0185-0724-10
Package Description: 1000 TABLET in 1 BOTTLE (0185-0724-10)

NDC Information of Carisoprodol and Aspirin

NDC Code 0185-0724-10
Proprietary Name Carisoprodol and Aspirin
Package Description 1000 TABLET in 1 BOTTLE (0185-0724-10)
Product NDC 0185-0724
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carisoprodol and Aspirin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960425
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name ASPIRIN; CARISOPRODOL
Strength Number 325; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC],Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Carisoprodol and Aspirin


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