Probenecid - 54868-0159-2 - (Probenecid)

Alphabetical Index


Drug Information of Probenecid

Product NDC: 54868-0159
Proprietary Name: Probenecid
Non Proprietary Name: Probenecid
Active Ingredient(s): 500    mg/1 & nbsp;   Probenecid
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Probenecid

Product NDC: 54868-0159
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084442
Marketing Category: ANDA
Start Marketing Date: 19950328

Package Information of Probenecid

Package NDC: 54868-0159-2
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (54868-0159-2)

NDC Information of Probenecid

NDC Code 54868-0159-2
Proprietary Name Probenecid
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (54868-0159-2)
Product NDC 54868-0159
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Probenecid
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19950328
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name PROBENECID
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Probenecid


General Information