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CARBIDOPA AND LEVODOPA - 62756-517-83 - (CARBIDOPA AND LEVODOPA)

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Drug Information of CARBIDOPA AND LEVODOPA

Product NDC: 62756-517
Proprietary Name: CARBIDOPA AND LEVODOPA
Non Proprietary Name: CARBIDOPA AND LEVODOPA
Active Ingredient(s): 10; 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: 62756-517
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078536
Marketing Category: ANDA
Start Marketing Date: 20081028

Package Information of CARBIDOPA AND LEVODOPA

Package NDC: 62756-517-83
Package Description: 30 TABLET in 1 BOTTLE (62756-517-83)

NDC Information of CARBIDOPA AND LEVODOPA

NDC Code 62756-517-83
Proprietary Name CARBIDOPA AND LEVODOPA
Package Description 30 TABLET in 1 BOTTLE (62756-517-83)
Product NDC 62756-517
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CARBIDOPA AND LEVODOPA
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081028
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name CARBIDOPA; LEVODOPA
Strength Number 10; 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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