Search by Drug Name or NDC

NDC 10135-0541-10 Probenecid 500 mg/1 Details

Probenecid 500 mg/1

Probenecid is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Marlex Pharmaceuticals Inc. The primary component is PROBENECID.

MedlinePlus Drug Summary

Probenecid is used to treat chronic gout and gouty arthritis. It is used to prevent attacks related to gout, not treat them once they occur. It acts on the kidneys to help the body eliminate uric acid. Probenecid is also used to make certain antibiotics more effective by preventing the body from passing them in the urine. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 10135-0541-10
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Probenecid

Product Information

NDC	10135-0541
Product ID	10135-541_0a37a2a4-a14d-cf40-e063-6394a90a736c
Associated GPIs	68100010000310
GCN Sequence Number	008236
GCN Sequence Number Description	probenecid TABLET 500 MG ORAL
HIC3	R1R
HIC3 Description	URICOSURIC AGENTS
GCN	35072
HICL Sequence Number	003675
HICL Sequence Number Description	PROBENECID
Brand/Generic	Generic
Proprietary Name	Probenecid
Proprietary Name Suffix	n/a
Non-Proprietary Name	Probenecid
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	PROBENECID
Labeler Name	Marlex Pharmaceuticals Inc
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA080966
Listing Certified Through	2024-12-31

Package

NDC 10135-0541-10 (10135054110)

Pricing Information	N/A
NDC Package Code	10135-541-10
Billing NDC	10135054110
Package	1000 TABLET, FILM COATED in 1 BOTTLE (10135-541-10)
Marketing Start Date	1976-07-29
NDC Exclude Flag	N