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Tiopronin

NDC 0480-7824 · Teva Pharmaceuticals, Inc.

Generic nameTiopronin
Dosage formTABLET, DELAYED RELEASE
RouteORAL
Active ingredient(s)TIOPRONIN
Strength300 mg/1
Pharmacologic classCystine Disulfide Reduction [MoA], N-substituted Glycines [CS], Reducing and Complexing Thiol [EPC]
Marketing categoryANDA

Packages

0480-7824-98 — 90 TABLET, DELAYED RELEASE in 1 BOTTLE (0480-7824-98)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0093-7909 — Tiopronin, 0178-0900 — tiopronin, 0178-0901 — tiopronin, 0178-0902 — tiopronin, 0254-3034 — TIOPRONIN, 0254-3035 — TIOPRONIN, 0480-9227 — Tiopronin, 13668-691 — tiopronin, 13668-692 — tiopronin, 44523-054 — Tiopronin, 44523-055 — Tiopronin, 60219-2009 — tiopronin, 70709-121 — tiopronin, 70709-123 — tiopronin

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels