NDC 71626-999

Probenecid

Probenecid

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

Product ID71626-999_0ffb25c6-72a5-4aa2-a389-1e57f0eb06de
NDC71626-999
Product TypeHuman Prescription Drug
Proprietary NameProbenecid
Generic NameProbenecid
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1976-07-29
Marketing CategoryANDA / ANDA
Application NumberANDA080966
Labeler NameMedstone Pharma LLC
Substance NamePROBENECID
Active Ingredient Strength500 mg/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 71626-999-08

8 TABLET, FILM COATED in 1 BOTTLE (71626-999-08)
Marketing Start Date2020-09-04
NDC Exclude FlagN
Sample Package?N

Drug Details

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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