Pioglitazone

NDC 70518-2129 · REMEDYREPACK INC.

Generic namePioglitazone

Dosage formTABLET

RouteORAL

Active ingredient(s)PIOGLITAZONE HYDROCHLORIDE

Strength30 mg/1

Pharmacologic classPeroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA], Peroxisome Proliferator-activated Receptor gamma Agonists [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]

Marketing categoryANDA

Packages

70518-2129-0 — 90 TABLET in 1 BOTTLE, PLASTIC (70518-2129-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

66993-821 — pioglitazone and glimepiride, 66993-822 — pioglitazone and glimepiride, 68071-2264 — Pioglitazone, 68071-2373 — Pioglitazone, 68071-4964 — Pioglitazone, 68071-5199 — Pioglitazone, 68071-5210 — Pioglitazone, 68071-5245 — Pioglitazone, 68788-7511 — Pioglitazone, 68788-7514 — Pioglitazone, 70518-2609 — Pioglitazone, 70518-4519 — pioglitazone hydrochloride, 71335-1298 — Pioglitazone, 71335-1333 — Pioglitazone, 71335-1343 — Pioglitazone, 71335-1759 — Pioglitazone, 71335-3019 — Pioglitazone and metformin hydrochloride, 71335-3020 — Pioglitazone and metformin hydrochloride, 71335-9664 — pioglitazone hydrochloride, 71610-495 — Pioglitazone, +68 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.