NDC 68682-200

Carbidopa

Carbidopa Tablets

Carbidopa is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Oceanside Pharmaceuticals. The primary component is Carbidopa.

Product ID68682-200_32765836-72d3-4eb4-9f96-589f9518d3be
NDC68682-200
Product TypeHuman Prescription Drug
Proprietary NameCarbidopa
Generic NameCarbidopa Tablets
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2014-04-04
Marketing CategoryNDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
Application NumberNDA017830
Labeler NameOceanside Pharmaceuticals
Substance NameCARBIDOPA
Active Ingredient Strength25 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68682-200-25

100 TABLET in 1 BOTTLE (68682-200-25)
Marketing Start Date2014-04-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68682-200-25 [68682020025]

Carbidopa TABLET
Marketing CategoryNDA authorized generic
Application NumberNDA017830
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-04-04

Drug Details

Active Ingredients

IngredientStrength
CARBIDOPA25 mg/1

OpenFDA Data

SPL SET ID:d5204e5e-10ef-4758-8fc6-cb710048c687
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 260260

    • Medicade Reported Pricing

    68682020025 CARBIDOPA 25 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Carbidopa" or generic name "Carbidopa Tablets"

    NDCBrand NameGeneric Name
    16714-067CarbidopaCarbidopa
    40032-980CarbidopaCarbidopa
    42799-123CarbidopaCarbidopa
    43386-980CarbidopaCarbidopa
    43975-220CarbidopaCarbidopa
    51407-314CarbidopaCarbidopa
    59651-146CarbidopaCarbidopa
    63629-1932CarbidopaCarbidopa
    63629-9193CarbidopaCarbidopa
    68682-200CarbidopaCarbidopa Tablets
    70710-1221CARBIDOPACARBIDOPA
    70771-1355CARBIDOPACARBIDOPA
    25010-711Lodosyncarbidopa
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