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Carbidopa and Levodopa - 62756-186-18 - (Carbidopa and Levodopa)

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Drug Information of Carbidopa and Levodopa

Product NDC: 62756-186
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, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Carbidopa and Levodopa

Product NDC: 62756-186
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078690
Marketing Category: ANDA
Start Marketing Date: 20090814

Package Information of Carbidopa and Levodopa

Package NDC: 62756-186-18
Package Description: 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62756-186-18)

NDC Information of Carbidopa and Levodopa

NDC Code 62756-186-18
Proprietary Name Carbidopa and Levodopa
Package Description 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62756-186-18)
Product NDC 62756-186
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbidopa and Levodopa
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20090814
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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