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Carbidopa and Levodopa - 55154-5975-9 - (Carbidopa and Levodopa)

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Drug Information of Carbidopa and Levodopa

Product NDC: 55154-5975
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
Coding System: National Drug Codes(NDC)

Labeler Information of Carbidopa and Levodopa

Product NDC: 55154-5975
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074260
Marketing Category: ANDA
Start Marketing Date: 19930903

Package Information of Carbidopa and Levodopa

Package NDC: 55154-5975-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-5975-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of Carbidopa and Levodopa

NDC Code 55154-5975-9
Proprietary Name Carbidopa and Levodopa
Package Description 6 BLISTER PACK in 1 CARTON (55154-5975-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-5975
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbidopa and Levodopa
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930903
Marketing Category Name ANDA
Labeler Name Cardinal Health
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


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