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Carbidopa-levodopa

NDC 52817-392 · TruPharma, LLC

Generic namecarbidopa and levodopa

Dosage formTABLET

RouteORAL

Active ingredient(s)CARBIDOPA, LEVODOPA

Strength25; 250 mg/1; mg/1

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

Marketing categoryANDA

Packages

52817-392-00 — 1000 TABLET in 1 BOTTLE (52817-392-00)

52817-392-10 — 100 TABLET in 1 BOTTLE (52817-392-10)

52817-392-50 — 500 TABLET in 1 BOTTLE (52817-392-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50228-457 — Carbidopa and Levodopa, 50228-458 — Carbidopa and Levodopa, 50228-459 — Carbidopa and Levodopa, 50228-460 — Carbidopa and Levodopa, 50228-461 — Carbidopa and Levodopa, 50268-202 — Carbidopa and Levodopa, 51079-923 — carbidopa and levodopa, 51079-978 — carbidopa and levodopa, 52817-390 — carbidopa and levodopa, 52817-391 — 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, 60687-661 — 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.