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Carbidopa and Levodopa

NDC 16571-157 · Rising Pharma Holdings, Inc.

Generic namecarbidopa and levodopa
Dosage formTABLET, ORALLY DISINTEGRATING
RouteORAL
Active ingredient(s)CARBIDOPA, LEVODOPA
Strength10; 100 mg/1; mg/1
Pharmacologic classAmino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]
Marketing categoryANDA

Packages

16571-157-01 — 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (16571-157-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0615-8555 — Carbidopa and Levodopa, 0781-5613 — Carbidopa, Levodopa, and Entacapone, 0781-5625 — Carbidopa, Levodopa, and Entacapone, 0781-5637 — Carbidopa, Levodopa, and Entacapone, 0781-5641 — Carbidopa, Levodopa, and Entacapone, 0781-5654 — Carbidopa, Levodopa, and Entacapone, 0781-5669 — Carbidopa, Levodopa, and Entacapone, 0904-7501 — Carbidopa and Levodopa, 0904-7549 — Carbidopa and Levodopa, 10144-342 — levodopa, 16571-158 — carbidopa and levodopa, 16571-159 — carbidopa and levodopa, 16571-689 — CARBIDOPA, LEVODOPA AND ENTACAPONE, 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, +147 more

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