NDC 68151-1993

Probenecid

Probenecid

Probenecid is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Carilion Materials Management. The primary component is Probenecid.

Product ID68151-1993_38db7765-dbeb-463a-a064-ece0c613780f
NDC68151-1993
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 NameCarilion Materials Management
Substance NamePROBENECID
Active Ingredient Strength500 mg/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 68151-1993-0

1 TABLET, FILM COATED in 1 PACKAGE (68151-1993-0)
Marketing Start Date1976-01-13
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68151-1993-0 [68151199300]

Probenecid TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA084211
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1976-01-13
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
PROBENECID500 mg/1

OpenFDA Data

SPL SET ID:8459857e-1a52-45de-81e6-e06ce18508bb
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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