NDC 70710-1210 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70710-1210

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210117
Marketed since
February 8, 2018
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
70710-1210-01000 TABLET in 1 BOTTLE (70710-1210-0)Feb 8, 2018
70710-1210-1100 TABLET in 1 BOTTLE (70710-1210-1)Feb 8, 2018
70710-1210-5500 TABLET in 1 BOTTLE (70710-1210-5)Feb 8, 2018

Other Allopurinol products