Pindolol

NDC 57664-655 · Sun Pharmaceutical Industries, Inc.

Generic namePindolol

Dosage formTABLET

RouteORAL

Active ingredient(s)PINDOLOL

Strength5 mg/1

Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Marketing categoryANDA

Packages

57664-655-88 — 100 TABLET in 1 BOTTLE, PLASTIC (57664-655-88)

FDA lists these products with the same active ingredient.

10135-743 — Pindolol, 10135-744 — Pindolol, 57664-656 — Pindolol, 62559-560 — Pindolol, 62559-561 — Pindolol, 63629-4828 — pindolol, 69367-421 — Pindolol, 69367-422 — Pindolol, 72162-2652 — Pindolol, 72162-2653 — Pindolol, 72789-099 — pindolol, 72789-100 — pindolol, 72789-293 — Pindolol, 72789-294 — Pindolol, 76385-131 — pindolol, 76385-132 — pindolol

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