NDC 68788-8337 – Allopurinol

Allopurinol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8337

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204467
Marketed since
January 23, 2023
Marketing end
September 29, 2027
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (4)

Package NDCDescriptionSince
68788-8337-1100 TABLET in 1 BOTTLE (68788-8337-1)Jan 23, 2023
68788-8337-330 TABLET in 1 BOTTLE (68788-8337-3)Jan 23, 2023
68788-8337-660 TABLET in 1 BOTTLE (68788-8337-6)Jan 23, 2023
68788-8337-990 TABLET in 1 BOTTLE (68788-8337-9)Jan 23, 2023

Other Allopurinol products