CARBIDOPA, LEVODOPA AND ENTACAPONE

NDC 16571-689 · Rising Pharma Holdings, Inc.

Generic nameCARBIDOPA, LEVODOPA AND ENTACAPONE

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)CARBIDOPA, LEVODOPA, ENTACAPONE

Strength12.5; 200; 50 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 categoryANDA

Packages

16571-689-01 — 100 TABLET, FILM COATED in 1 BOTTLE (16571-689-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0781-5641 — 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, 16571-690 — CARBIDOPA, LEVODOPA AND ENTACAPONE, 16571-691 — CARBIDOPA, LEVODOPA AND ENTACAPONE, 16571-692 — CARBIDOPA, LEVODOPA AND ENTACAPONE, 16571-693 — CARBIDOPA, LEVODOPA AND ENTACAPONE, 16571-694 — CARBIDOPA, LEVODOPA AND ENTACAPONE, 16714-067 — Carbidopa, 16729-078 — Carbidopa and Levodopa, 16729-079 — Carbidopa and Levodopa, 25010-711 — carbidopa, 27241-049 — Entacapone, +162 more

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