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Carbidopa and Levodopa - 52125-096-02 - (Carbidopa and Levodopa)

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Drug Information of Carbidopa and Levodopa

Product NDC: 52125-096
Proprietary Name: Carbidopa and Levodopa
Non Proprietary Name: Carbidopa and Levodopa
Active Ingredient(s): 10    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: 52125-096
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073618
Marketing Category: ANDA
Start Marketing Date: 20130222

Package Information of Carbidopa and Levodopa

Package NDC: 52125-096-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-096-02)

NDC Information of Carbidopa and Levodopa

NDC Code 52125-096-02
Proprietary Name Carbidopa and Levodopa
Package Description 30 TABLET in 1 BLISTER PACK (52125-096-02)
Product NDC 52125-096
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbidopa and Levodopa
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130222
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name CARBIDOPA
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Carbidopa and Levodopa


General Information