NDC 0527-1367 – Probenecid

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

Human Prescription Drug

Product NDC0527-1367

Product details

Brand name
Probenecid
Generic name
Probenecid
Labeler
Lannett Company, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA080966
Marketed since
July 29, 1976
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Probenecid →

Package NDC codes (2)

Package NDCDescriptionSince
0527-1367-01100 TABLET, FILM COATED in 1 BOTTLE (0527-1367-01)Jul 29, 1976
0527-1367-101000 TABLET, FILM COATED in 1 BOTTLE (0527-1367-10)Jul 29, 1976

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