NDC 31722-252 – Allopurinol

Allopurinol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC31722-252

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA217748
Marketed since
August 3, 2023
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (4)

Package NDCDescriptionSince
31722-252-01100 TABLET in 1 BOTTLE (31722-252-01)Aug 3, 2023
31722-252-05500 TABLET in 1 BOTTLE (31722-252-05)Aug 3, 2023
31722-252-101000 TABLET in 1 BOTTLE (31722-252-10)Aug 3, 2023
31722-252-9090 TABLET in 1 BOTTLE (31722-252-90)Aug 3, 2023

Other Allopurinol products