NDC 43353-991

Probenecid

Probenecid

Probenecid is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Aphena Pharma Solutions - Tennessee, Llc. The primary component is Probenecid.

Product ID43353-991_169cd45c-f0a8-4fe7-a1e1-e6362b5c719c
NDC43353-991
Product TypeHuman Prescription Drug
Proprietary NameProbenecid
Generic NameProbenecid
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1976-01-13
Marketing CategoryANDA / ANDA
Application NumberANDA084211
Labeler NameAphena Pharma Solutions - Tennessee, LLC
Substance NamePROBENECID
Active Ingredient Strength500 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 43353-991-60

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-991-60)
Marketing Start Date2015-01-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43353-991-60 [43353099160]

Probenecid TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA084211
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-01-12

Drug Details

Active Ingredients

IngredientStrength
PROBENECID500 mg/1

OpenFDA Data

SPL SET ID:1bfc27ef-d061-43b5-a3d2-a39b15c6e1f8
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198152
  • NDC Crossover Matching brand name "Probenecid" or generic name "Probenecid"

    NDCBrand NameGeneric Name
    0378-0156Probenecidprobenecid
    0527-1367ProbenecidProbenecid
    0591-5347ProbenecidProbenecid
    10135-541ProbenecidProbenecid
    11819-282ProbenecidProbenecid
    43353-839ProbenecidProbenecid
    43353-991Probenecidprobenecid
    63629-8213ProbenecidProbenecid
    68084-945ProbenecidProbenecid
    68151-1993Probenecidprobenecid
    69367-154ProbenecidProbenecid
    71335-1697ProbenecidProbenecid
    71626-999ProbenecidProbenecid

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