Carbidopa, Levodopa, and Entacapone

NDC 0781-5641 · Sandoz Inc

Generic nameCarbidopa, Levodopa, and Entacapone

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)CARBIDOPA, LEVODOPA, ENTACAPONE

Strength31.25; 200; 125 mg/1; mg/1; mg/1

Pharmacologic classAmino Acids, Aromatic [CS], Aromatic Amino Acid [EPC], Catechol O-Methyltransferase Inhibitors [MoA], Catechol-O-Methyltransferase Inhibitor [EPC]

Marketing categoryNDA AUTHORIZED GENERIC

Packages

0781-5641-01 — 100 TABLET, FILM COATED in 1 BOTTLE (0781-5641-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0615-8298 — Entacapone, 0615-8460 — Carbidopa and Levodopa, 0615-8461 — Carbidopa and Levodopa, 0615-8516 — Carbidopa and Levodopa, 0615-8536 — Carbidopa and Levodopa, 0615-8555 — Carbidopa and Levodopa, 0781-5578 — Entacapone, 0781-5613 — Carbidopa, Levodopa, and Entacapone, 0781-5625 — Carbidopa, Levodopa, and Entacapone, 0781-5637 — Carbidopa, Levodopa, and Entacapone, 0781-5654 — Carbidopa, Levodopa, and Entacapone, 0781-5669 — Carbidopa, Levodopa, and Entacapone, 0904-6822 — Entacapone, 0904-7501 — Carbidopa and Levodopa, 0904-7549 — Carbidopa and Levodopa, 10144-342 — levodopa, 16571-157 — carbidopa and levodopa, 16571-158 — carbidopa and levodopa, 16571-159 — carbidopa and levodopa, 16571-689 — CARBIDOPA, LEVODOPA AND ENTACAPONE, +174 more

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