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Carbidopa and levodopa - 43353-510-80 - (Carbidopa and levodopa)

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Drug Information of Carbidopa and levodopa

Product NDC: 43353-510
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: 43353-510
Labeler Name: Aphena Pharma Solutions - Tennessee, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074260
Marketing Category: ANDA
Start Marketing Date: 19930901

Package Information of Carbidopa and levodopa

Package NDC: 43353-510-80
Package Description: 180 TABLET in 1 BOTTLE, PLASTIC (43353-510-80)

NDC Information of Carbidopa and levodopa

NDC Code 43353-510-80
Proprietary Name Carbidopa and levodopa
Package Description 180 TABLET in 1 BOTTLE, PLASTIC (43353-510-80)
Product NDC 43353-510
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbidopa and levodopa
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930901
Marketing Category Name ANDA
Labeler Name Aphena Pharma Solutions - Tennessee, 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]

Complete Information of Carbidopa and levodopa


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