NDC 70710-1221

CARBIDOPA

Carbidopa

CARBIDOPA is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Zydus Pharmaceuticals (usa) Inc.. The primary component is Carbidopa.

Product ID70710-1221_3987b433-3414-4b64-9d58-3d90b5e091db
NDC70710-1221
Product TypeHuman Prescription Drug
Proprietary NameCARBIDOPA
Generic NameCarbidopa
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2018-09-06
Marketing CategoryANDA / ANDA
Application NumberANDA209910
Labeler NameZydus Pharmaceuticals (USA) Inc.
Substance NameCARBIDOPA
Active Ingredient Strength25 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 70710-1221-1

100 TABLET in 1 BOTTLE (70710-1221-1)
Marketing Start Date2018-09-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70710-1221-1 [70710122101]

CARBIDOPA TABLET
Marketing CategoryANDA
Application NumberANDA209910
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-09-06

Drug Details

Active Ingredients

IngredientStrength
CARBIDOPA25 mg/1

OpenFDA Data

SPL SET ID:c0b1ef99-3092-431a-8fb6-897affd52595
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 260260

    • 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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