NDC 69367-154

Probenecid

Probenecid

Probenecid is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Westminster Pharmaceuticals, Llc. The primary component is Probenecid.

Product ID69367-154_38a2d4c1-e32a-2dbb-e054-00144ff8d46c
NDC69367-154
Product TypeHuman Prescription Drug
Proprietary NameProbenecid
Generic NameProbenecid
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-07-28
Marketing CategoryANDA / ANDA
Application NumberANDA084442
Labeler NameWestminster Pharmaceuticals, LLC
Substance NamePROBENECID
Active Ingredient Strength500 mg/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 69367-154-00

8 TABLET in 1 BOTTLE (69367-154-00)
Marketing Start Date2016-07-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69367-154-00 [69367015400]

Probenecid TABLET
Marketing CategoryANDA
Application NumberANDA084442
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-07-28
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
PROBENECID500 mg/1

OpenFDA Data

SPL SET ID:38a2d4c1-e329-2dbb-e054-00144ff8d46c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198152
  • UPC Code
  • 0369367154000
  • 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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