NDC 0591-5347 – Probenecid

Probenecid 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0591-5347

Product details

Brand name
Probenecid
Generic name
Probenecid
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA084442
Marketed since
July 1, 1983
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Probenecid →

Package NDC codes (2)

Package NDCDescriptionSince
0591-5347-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-5347-01)Jul 1, 1983
0591-5347-101000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-5347-10)Jul 1, 1983

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