Skip to main content

Carbidopa and Levodopa

NDC 60687-661 · American Health Packaging

Generic nameCarbidopa and Levodopa

Dosage formTABLET

RouteORAL

Active ingredient(s)CARBIDOPA, LEVODOPA

Strength25; 100 mg/1; mg/1

Pharmacologic classAmino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]

Marketing categoryANDA

Packages

60687-661-01 — 100 BLISTER PACK in 1 CARTON (60687-661-01) / 1 TABLET in 1 BLISTER PACK (60687-661-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

52817-392 — carbidopa and levodopa, 53401-020 — Carbidopa and Levodopa, 55154-0192 — Carbidopa and Levodopa, 55154-2643 — Carbidopa and Levodopa, 59651-146 — Carbidopa, 59651-456 — Carbidopa and Levodopa, 59651-457 — Carbidopa and Levodopa, 59651-458 — Carbidopa and Levodopa, 60219-2033 — CARBIDOPA and LEVODOPA, 60219-2034 — CARBIDOPA and LEVODOPA, 60687-836 — Carbidopa and Levodopa, 62332-332 — Carbidopa and Levodopa, 62332-333 — Carbidopa and Levodopa, 62332-795 — carbidopa, levodopa and entacapone, 62332-796 — carbidopa, levodopa and entacapone, 62332-797 — carbidopa, levodopa and entacapone, 62332-798 — carbidopa, levodopa and entacapone, 62332-799 — carbidopa, levodopa and entacapone, 62332-800 — carbidopa, levodopa and entacapone, 62756-457 — 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.