Home > National Drug Code (NDC) > Carbidopa and Levodopa

Carbidopa and Levodopa - 54868-5659-0 - (Carbidopa and Levodopa)

Alphabetical Index


Drug Information of Carbidopa and Levodopa

Product NDC: 54868-5659
Proprietary Name: Carbidopa and Levodopa
Non Proprietary Name: Carbidopa and Levodopa
Active Ingredient(s): 25; 100    mg/1; mg/1 & nbsp;   Carbidopa and Levodopa
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Carbidopa and Levodopa

Product NDC: 54868-5659
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077828
Marketing Category: ANDA
Start Marketing Date: 20060818

Package Information of Carbidopa and Levodopa

Package NDC: 54868-5659-0
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-5659-0)

NDC Information of Carbidopa and Levodopa

NDC Code 54868-5659-0
Proprietary Name Carbidopa and Levodopa
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-5659-0)
Product NDC 54868-5659
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbidopa and Levodopa
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060818
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CARBIDOPA; LEVODOPA
Strength Number 25; 100
Strength Unit mg/1; mg/1
Pharmaceutical Classes Aromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA],Aromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA]

Complete Information of Carbidopa and Levodopa


General Information