NDC 71205-377 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-377

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071450
Marketed since
January 9, 1987
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (3)

Package NDCDescriptionSince
71205-377-3030 TABLET in 1 BOTTLE, PLASTIC (71205-377-30)Dec 26, 2019
71205-377-6060 TABLET in 1 BOTTLE, PLASTIC (71205-377-60)Dec 26, 2019
71205-377-9090 TABLET in 1 BOTTLE, PLASTIC (71205-377-90)Dec 26, 2019

Other Allopurinol products