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Carbidopa and Levodopa - 76237-259-30 - (carbidopa and levodopa)

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Drug Information of Carbidopa and Levodopa

Product NDC: 76237-259
Proprietary Name: Carbidopa and Levodopa
Non Proprietary Name: carbidopa and levodopa
Active Ingredient(s): 50; 200    mg/1; mg/1 & nbsp;   carbidopa and levodopa
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Carbidopa and Levodopa

Product NDC: 76237-259
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075091
Marketing Category: ANDA
Start Marketing Date: 20120208

Package Information of Carbidopa and Levodopa

Package NDC: 76237-259-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-259-30) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Carbidopa and Levodopa

NDC Code 76237-259-30
Proprietary Name Carbidopa and Levodopa
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-259-30) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 76237-259
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name carbidopa and levodopa
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120208
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name CARBIDOPA; LEVODOPA
Strength Number 50; 200
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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