NDC 16714-067

Carbidopa

Carbidopa

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

Product ID16714-067_33ee4598-cbcc-45e0-a48e-dc0101e1f204
NDC16714-067
Product TypeHuman Prescription Drug
Proprietary NameCarbidopa
Generic NameCarbidopa
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2019-10-21
Marketing CategoryANDA / ANDA
Application NumberANDA211055
Labeler NameNorthStar Rx LLC
Substance NameCARBIDOPA
Active Ingredient Strength25 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 16714-067-01

100 TABLET in 1 BOTTLE (16714-067-01)
Marketing Start Date2019-10-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 16714-067-01 [16714006701]

Carbidopa TABLET
Marketing CategoryANDA
Application NumberANDA211055
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
CARBIDOPA25 mg/1

OpenFDA Data

SPL SET ID:33ee4598-cbcc-45e0-a48e-dc0101e1f204
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 260260
  • Medicade Reported Pricing

    16714067102 ONDANSETRON 4 MG/5 ML SOLUTION

    Pricing Unit: ML | Drug Type:

    16714067101 ONDANSETRON 4 MG/5 ML SOLUTION

    Pricing Unit: ML | 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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