FDA.reportPublic FDA data

NDC 0091-3341 - Parcopa

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
0091-3341
Package NDCs from labels
0091-3341-01
Manufacturer
Schwarz Pharma
Effective date
2007-11-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Parcopa - Schwarz PharmaSchwarz Pharma2007-11-05Human prescription drug label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0091-3341-01Parcopa100 in 1 BOTTLETABLET, ORALLY DISINTEGRATING1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0091-3341PARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]21 package rows20071130_E1FF4C1F-5D6F-44A6-A0F6-D7CA2A94ADB9.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CarbidopaACTIVE INGREDIENTMNX7R8C5VOPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
LevodopaACTIVE INGREDIENT46627O600JPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
CarbidopaACTIVE MOIETYMNX7R8C5VOPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
LevodopaACTIVE MOIETY46627O600JPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
Artificial Mint FlavorINACTIVE INGREDIENTPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
AspartameINACTIVE INGREDIENTPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
Citric AcidINACTIVE INGREDIENT2968PHW8QPPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
CrospovidoneINACTIVE INGREDIENTPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
FD&C Blue #2 HT Aluminum LakeINACTIVE INGREDIENTPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
FDC Blue #2 HT Aluminum LakeINACTIVE INGREDIENTPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
Magnesium StearateINACTIVE INGREDIENT70097M6I30PARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
MannitolINACTIVE INGREDIENT3OWL53L36APARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
Microcrystalline CelluloseINACTIVE INGREDIENTPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
Natural Mint FlavorINACTIVE INGREDIENTPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
Sodium BicarbonateINACTIVE INGREDIENT8MDF5V39QOPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2
Yellow 10 Iron OxideINACTIVE INGREDIENTPARCOPA (CARBIDOPA AND LEVODOPA) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA]2

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 ยท 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CARBIDOPA AND LEVODOPACARBIDOPA AND LEVODOPASun Pharmaceutical Industries, Inc.48e0f2ec-b217-4c25-a71c-20e173d05edb2026-06-12Warnings, Adverse reactionsExact identifier
rxcui: 476515
rxcui: 483090
rxcui: 476399
Carbidopa and LevodopaCARBIDOPA AND LEVODOPARising Pharma Holdings, Inc.302bfe03-d222-4a87-80ff-f2dbfb9a07f42026-01-27Warnings, Adverse reactionsExact identifier
rxcui: 476515
rxcui: 483090
rxcui: 476399
9DBBE60D-658A-0C7F-4F94-26961268C24AE1FF4C1F-5D6F-44A6-A0F6-D7CA2A94ADB92007-11-05Warnings, Adverse reactionsExact identifier
spl id: 9DBBE60D-658A-0C7F-4F94-26961268C24A
spl set id: E1FF4C1F-5D6F-44A6-A0F6-D7CA2A94ADB9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.