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Carbidopa and Levodopa - 0904-7719-61 - (Carbidopa and Levodopa)

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Drug Information of Carbidopa and Levodopa

Product NDC: 0904-7719
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: 0904-7719
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073589
Marketing Category: ANDA
Start Marketing Date: 20110519

Package Information of Carbidopa and Levodopa

Package NDC: 0904-7719-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-7719-61)

NDC Information of Carbidopa and Levodopa

NDC Code 0904-7719-61
Proprietary Name Carbidopa and Levodopa
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-7719-61)
Product NDC 0904-7719
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbidopa and Levodopa
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110519
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
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]

Complete Information of Carbidopa and Levodopa


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