NDC 43975-220

Carbidopa

Carbidopa

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

Product ID43975-220_093c7ccd-9e02-42ac-84a6-9e62923e42a4
NDC43975-220
Product TypeHuman Prescription Drug
Proprietary NameCarbidopa
Generic NameCarbidopa
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2014-03-10
Marketing CategoryANDA / ANDA
Application NumberANDA203261
Labeler NameANI Pharmaceuticals, Inc.
Substance NameCARBIDOPA
Active Ingredient Strength25 mg/1
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 43975-220-10

100 TABLET in 1 BOTTLE (43975-220-10)
Marketing Start Date2014-03-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43975-220-10 [43975022010]

Carbidopa TABLET
Marketing CategoryANDA
Application NumberANDA203261
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-03-10

Drug Details

Active Ingredients

IngredientStrength
CARBIDOPA25 mg/1

OpenFDA Data

SPL SET ID:c47856c9-7013-44a2-b381-4ca67e1d1b4c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 260260

    • Medicade Reported Pricing

    43975022010 CARBIDOPA 25 MG TABLET

    Pricing Unit: EA | Drug Type:

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

    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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