SINEMET - 0006-3919-68 - (carbidopa and levodopa)

Alphabetical Index


Drug Information of SINEMET

Product NDC: 0006-3919
Proprietary Name: SINEMET
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 SINEMET

Product NDC: 0006-3919
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019856
Marketing Category: NDA
Start Marketing Date: 19910530

Package Information of SINEMET

Package NDC: 0006-3919-68
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0006-3919-68)

NDC Information of SINEMET

NDC Code 0006-3919-68
Proprietary Name SINEMET
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0006-3919-68)
Product NDC 0006-3919
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name carbidopa and levodopa
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19910530
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
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 SINEMET


General Information